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GERMANY

Nordrhein-Westfalen
MÖNCHENGLADBACH

Accreditation
Biochemical diagnosis of congenital plasminogen activator inhibitor type 1 deficiency
Medizinische Versorgungszentrum Dr.Stein + Kollegen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Biochemical genetics
Objective(s) : Analyte / Enzyme assay

BELGIUM

ANTWERPEN
ANTWERPEN-EDEGEM

Accreditation
Molecular diagnosis of APC resistance due to Factor V Leiden (F5 gene)
University Hospital of Antwerp - UZA- Centrum Medische Genetica - CMG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Lanarkshire
GLASGOW

Accreditation
Molecular diagnosis of hyperprothrombinemia (Prothrombin 20210A mutation)
Southern General Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

AUSTRIA

OBERÖSTERREICH
LINZ

Accreditation
Molecular diagnosis of non rare thrombophilia (F5: Leiden mutation (G1691A); F2: G20210A; MTHFR: C677T and A1298C)
Krankenhaus der Barmherzigen Schwestern Linz
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Wiltshire
SALISBURY

Accreditation
Molecular diagnosis of Factor V Deficiency - Leiden (F5: specific mutation analysis)
Salisbury District Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Wiltshire
SALISBURY

Accreditation
Molecular diagnosis of Hyperprothrombinemia (Prothrombin 20210A mutation)
Salisbury District Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
IVRY SUR SEINE

Accreditation
Molecular diagnosis of MTHFR thermolabile variant (C677T mutation)
Eurofins Biomnis
Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technical procedure(s) : PCR based techniques

UNITED KINGDOM

Greater London
HARROW

Accreditation
Molecular diagnosis of hyperprothrombinemia (Prothrombin 20210A, F2 gene)
North West London Hospitals NHS - Northwick Park & St Marks Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Rheinland-Pfalz
INGELHEIM AM RHEIN

Accreditation
Molecular diagnosis of MTHFR gene variant C677T
Bioscientia Institut für Medizinische Diagnostik GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Rheinland-Pfalz
INGELHEIM AM RHEIN

Accreditation
Molecular diagnosis of congential plasminogen activator inhibitor type 1 deficiency
Bioscientia Institut für Medizinische Diagnostik GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Nordrhein-Westfalen
KÖLN

Accreditation
Molecular diagnosis of MTHFR gene variant C677T
Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
KÖLN

Accreditation
Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the PAI1 gene)
Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MÜNCHEN

Accreditation
Molecular diagnosis of MTHFR gene variants C677T and C677T
Zweigniederlassung der synlab MVZ Augsburg GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
NEU-ULM

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Paxis und Labor Dr. med Karl Mehnert
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
NEU-ULM

Accreditation
Molecular diagnosis of factor V Leiden mutation
Paxis und Labor Dr. med Karl Mehnert
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Molecular diagnosis of factor V Leiden mutation
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Molecular diagnosis of MTHFR gene variant C677T, A1298C
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Grampian
ABERDEEN

Accreditation
Molecular diagnosis of Factor V Deficiency (Leiden)
Aberdeen Royal Infirmary, Polwarth Building
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Grampian
ABERDEEN

Accreditation
Molecular diagnosis of hyperprothrombinemia (Prothrombin 20210A mutation)
Aberdeen Royal Infirmary, Polwarth Building
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Greater London
LONDON

Accreditation
Molecular diagnosis of Factor V deficiency (Leiden plus complete F5 gene)
St Thomas' Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Greater London
LONDON

Accreditation
Molecular diagnosis of Methylenetetrahydrofolate Reductase Deficiency (MTHFR), thermolabile variant (C677T)
St Thomas' Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Greater London
LONDON

Accreditation
Molecular diagnosis of Congenital Factor II deficiency (20210A plus complete Prothrombin gene)
St Thomas' Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Cataluña
BARCELONA

Accreditation
Molecular diagnosis of predisposition to thrombophilia. F5 gene.
Laboratorio de Análisis Dr. Echevarne
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular diagnosis of factor V Leiden mutation
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MARTINSRIED

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MÜNCHEN

Accreditation
Molecular diagnosis of factor V Leiden mutation
Zweigniederlassung der synlab MVZ Augsburg GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

AUSTRIA

TIROL
INNSBRUCK

Accreditation
Molecular diagnosis of Factor V Leiden mutation
Medizinische Universität Innsbruck
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

BELGIUM

HAINAUT
GOSSELIES

Accreditation
Molecular diagnosis of non-rare thrombophilia (Factor 2 20210G>A variant)
Institut de Pathologie et de Génétique - Gosselies
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Niedersachsen
GÖTTINGEN

Accreditation
Molecular diagnosis of MTHFR gene variants C677T and A1298C
Institut für Humangenetik der Universität Göttingen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing

GERMANY

Rheinland-Pfalz
MAINZ

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Institut für Klinische Genetik Mainz
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Rheinland-Pfalz
MAINZ

Accreditation
Molecular diagnosis of factor V Leiden mutation
Institut für Klinische Genetik Mainz
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Rheinland-Pfalz
MAINZ

Accreditation
Molecular diagnosis of MTHFR gene variant C677T
Institut für Klinische Genetik Mainz
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the SERPINE1 gene)
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Sachsen
WEIßWASSER

Accreditation
Molecular diagnosis of factor V deficiency and resistance to activated protein C (F5 gene: fragment analysis and sequencing of selective regions)
Praxis Dr. Mato Nagel
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

UNITED KINGDOM

Devon
PLYMOUTH

Accreditation
Molecular diagnosis of hyperprothrombinemia (Prothrombin 20210A mutation)
Plymouth Derriford Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Devon
PLYMOUTH

Accreditation
Molecular diagnosis of Congenital Factor V Deficiency (Leiden, F5 gene G617A mutation)
Plymouth Derriford Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Sachsen
DRESDEN

Accreditation
Molecular diagnosis of thrombophilia (F5: factor V Leiden mutation, factor V Cambridge mutation, and others)
Mitteldeutscher Praxisverbund Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
MÖNCHENGLADBACH

Accreditation
Molecular diagnosis of factor V Leiden mutation
Medizinische Versorgungszentrum Dr.Stein + Kollegen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MÜNCHEN

Accreditation
Molecular diagnosis of factor V Leiden mutation (QF-PCR)
Pränatalmedizin München
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

GERMANY

Bayern
MÜNCHEN

Accreditation
Molecular diagnosis of factor V Leiden mutation
Medizinisch Genetisches Zentrum München
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing

GERMANY

Nordrhein-Westfalen
KÖLN

Accreditation
Molecular diagnosis of factor V Leiden mutation
Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Schleswig-Holstein
KIEL

Accreditation
Molecular diagnosis of factor V Leiden mutation
Universitätsklinikum Schleswig-Holstein - Campus Kiel
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing

GERMANY

Rheinland-Pfalz
INGELHEIM AM RHEIN

Accreditation
Molecular diagnosis of factor V Leiden mutation
Bioscientia Institut für Medizinische Diagnostik GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
MÖNCHENGLADBACH

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Medizinische Versorgungszentrum Dr.Stein + Kollegen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Rheinland-Pfalz
INGELHEIM AM RHEIN

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Bioscientia Institut für Medizinische Diagnostik GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the PAI1 gene)
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
SAINT-OUEN-L'AUMÔNE

Accreditation
Diagnostic of susceptibility to non rare thrombophilia (mutations R506Q, G20210A, C677T variant)
Laboratoire Cerba
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation
Molecular diagnosis of factor V Leiden mutation
Centogene AG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Centogene AG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MÜNCHEN

Accreditation
Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the PAI1 gene)
Zweigniederlassung der synlab MVZ Augsburg GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Avon
BRISTOL

Accreditation
Molecular diagnosis of resistance to activated protein C - Factor V Leiden (F5 gene, G1691A mutation)
Southmead Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
MÖNCHENGLADBACH

Accreditation
Molecular diagnosis of MTHFR gene variant C677T
Medizinische Versorgungszentrum Dr.Stein + Kollegen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Schleswig-Holstein
KIEL

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Universitätsklinikum Schleswig-Holstein - Campus Kiel
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing

FINLAND

Finland
HELSINKI

Accreditation
Molecular diagnosis of hyperprothrombinemia (F2 gene: G20210A mutation)
Yhtyneet Medix Laboratoriot
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FINLAND

Finland
HELSINKI

Accreditation
Molecular diagnosis of factor V deficiency (F5 gene: G1691A mutation)
Yhtyneet Medix Laboratoriot
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Niedersachsen
HANNOVER

Accreditation
Molecular diagnosis of MTHFR gene variant C677T
Medizinische Hochschule Hannover
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Sachsen
LEIPZIG

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
MVZ Labor Dr. Reising-Ackermann und Kollegen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Sachsen
LEIPZIG

Accreditation
Molecular diagnosis of thrombophilia (F5: factor V Leiden mutation, factor V Cambridge mutation, H1299R)
MVZ Labor Dr. Reising-Ackermann und Kollegen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Sachsen
LEIPZIG

Accreditation
Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the SERPINE1 gene)
MVZ Labor Dr. Reising-Ackermann und Kollegen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Diagenom GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hamburg
HAMBURG

Accreditation
Molecular diagnosis of factor V Leiden mutation
amedes genetics im MVZ für Labormedizin und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hamburg
HAMBURG

Accreditation
Molecular diagnosis of MTHFR gene variant C677T
amedes genetics im MVZ für Labormedizin und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

NORD-PAS-DE-CALAIS
VALENCIENNES

Accreditation
Molecular diagnosis of thrombosis risks (F2 gene: G20210A mutation; F5 gene: Leiden mutation; MTHFR gene)
Centre Hospitalier de Valenciennes
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

GERMANY

Niedersachsen
GÖTTINGEN

Accreditation
Molecular diagnosis of factor V Leiden mutation
Institut für Humangenetik der Universität Göttingen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing

GERMANY

Niedersachsen
GÖTTINGEN

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Institut für Humangenetik der Universität Göttingen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing

GERMANY

Hamburg
HAMBURG

Accreditation
Molecular diagnosis of factor V deficiency and resistance to activated protein C
Labor Lademannbogen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hamburg
HAMBURG

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation, PROZ, SERPINA10 gene)
Labor Lademannbogen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Hamburg
HAMBURG

Accreditation
Molecular diagnosis of MTHFR gene variant C677T
Labor Lademannbogen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GREECE

ATTIKI
ATHENS

Accreditation
Molecular diagnosis of resistance to activated protein C (F5 gene: R506Q mutation)
BioAnalytica-GenoType SA
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GREECE

ATTIKI
ATHENS

Accreditation
Molecular diagnosis of hyperprothrombinemia (F2 gene: G20210A mutation)
BioAnalytica-GenoType SA
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GREECE

ATTIKI
ATHENS

Accreditation
Molecular diagnosis of MTHFR deficiency (C677T and A1298C mutations)
BioAnalytica-GenoType SA
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MÜNCHEN

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Medizinisch Genetisches Zentrum München
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing

UNITED KINGDOM

South Glamorgan
CARDIFF

Accreditation
Molecular diagnosis of MTHFR deficiency due to C667T thermolabile variant
University Hospital of Wales
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hamburg
HAMBURG

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
amedes genetics im MVZ für Labormedizin und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

BELGIUM

VLAAMS BRABANT
LEUVEN

Accreditation
Molecular diagnosis of Non rare thrombophilia (R506Q - Factor V Leiden)
University Hospitals Leuven - Gasthuisberg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

BELGIUM

VLAAMS BRABANT
LEUVEN

Accreditation
Molecular diagnosis of Non rare thrombophilia (Factor II 20210G>A variant)
University Hospitals Leuven - Gasthuisberg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

BELGIUM

VLAAMS BRABANT
LEUVEN

Accreditation
Molecular diagnosis of Non rare thrombophilia (MTHFR C677T variant)
University Hospitals Leuven - Gasthuisberg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

PROVENCE-ALPES-COTE D'AZUR
NICE

Accreditation
Molecular diagnosis of non rare thrombophilia (F5 gene: Leiden mutation; F2 gene: G20210A mutation)
CHU de Nice - Hôpital Pasteur
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

SWITZERLAND

Suisse Italienne
LUGANO

Accreditation
Molecular diagnosis of resistance to activated protein C
Procrea Lab SA - Laboratorio di Genetica Molecolare
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SWITZERLAND

Suisse Italienne
LUGANO

Accreditation
Molecular diagnosis of Congenital factor II deficiency
Procrea Lab SA - Laboratorio di Genetica Molecolare
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ESTONIA

Tartu
TARTU

Accreditation
Molecular diagnosis of non rare thrombophilia (F5 gene: Leiden mutation, F2 gene: G20210A variant, MTHFR gene: C667T and A1298C variants)
Asper Biotech Ltd.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

Accreditation
Molecular diagnosis of thrombophilia: factor V Leiden (F5 gene: R534Q (p.R506Q) mutation) and factor II (F2 gene G20210A mutation)
Addenbrooke's Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SWITZERLAND

Suisse Alémanique
ZÜRICH

Accreditation
Molecular diagnosis of factor V deficiency and resistance to activaded protein C (F5 gene)
Genetica AG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
IVRY SUR SEINE

Accreditation
Molecular diagnosis of non rare thrombophilia (F2, F5, MTHFR genes)
Eurofins Biomnis
Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

GERMANY

Nordrhein-Westfalen
KÖLN

Accreditation
Molecular diagnosis of non rare thrombophilia (FII, FV, MTHFR genes)
Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Sachsen
DRESDEN

Accreditation
Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the PAI1 gene)
Mitteldeutscher Praxisverbund Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

AUSTRIA

STEIERMARK
GRAZ

Accreditation
Molecular diagnosis of non-rare thrombophilia (factor V-Leiden mutation)
Medizinische Universität Graz
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation
Molecular diagnosis of non rare thrombophilia (MTHFR gene)
CHU de Marseille - Hôpital de la Timone
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

GERMANY

Bayern
MÜNCHEN

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Zweigniederlassung der synlab MVZ Augsburg GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

AUSTRIA

TIROL
INNSBRUCK

Accreditation
Molecular diagnosis of hereditary thrombophilia (F2 gene)
Medizinische Universität Innsbruck
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Lanarkshire
GLASGOW

Accreditation
Molecular diagnosis of non rare thrombophilia (F5 gene: G1691A mutation)
Southern General Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Molecular diagnosis of non rare thrombophilia (MTHFR gene)
CHU Paris IdF Ouest - HEGP Hôpital Européen Georges Pompidou
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

CANADA

Ontario
MISSISSAUGA

Accreditation
Molecular Diagnosis of Thrombophilia Susceptibility
Trillium Health Partners- Credit Valley Site
Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

SWITZERLAND

Suisse Romande
GENÈVE

Accreditation
Molecular diagnosis of non rare thrombophilia: factor II (gene F2 mutation G20210A)
Hôpitaux Universitaires de Genève HUG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SWITZERLAND

Suisse Romande
GENÈVE

Accreditation
Molecualr diagnosis of non rare thrombophilia (F5 gene: Leiden (R506Q) mutation detection)
Hôpitaux Universitaires de Genève HUG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SWITZERLAND

Suisse Romande
LAUSANNE

Accreditation
Molecular diagnosis of non rare thrombophilia (F2 gene, F5 gene)
Synlab Lausanne
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MÜNCHEN

Accreditation
Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the PAI1 gene)
Zweigniederlassung der synlab MVZ Augsburg GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CANADA

Ontario
OTTAWA

Accreditation
Molecular Diagnosis of Non-Rare Thrombophilia (F2, FV targeted mutation analysis)
Children's Hospital of Eastern Ontario
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Familial Thrombosis (FVL, F2 targeted mutation analysis)
North York General Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Predisposition to Thrombophilia (FVL, F2 g.20210G>A, MTHFR c.677 C>T)
Mount Sinai Hospital
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MÜNCHEN

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Pränatalmedizin München
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MÜNCHEN

Accreditation
Molecular diagnosis of MTHFR deficiency (MTHFR gene)
Pränatalmedizin München
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technical procedure(s) : Sanger sequencing, MLPA based techniques

GERMANY

Baden-Württemberg
TÜBINGEN

Accreditation
Molecular diagnosis of non rare thrombophilia (F2, F5, F12 genes: sequencing)
CeGaT GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

FRANCE

RHONE-ALPES
LYON

Accreditation
Diagnosis of non rare thrombophilia (F5 and F2 genes)
Eurofins Biomnis
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
SURESNES

Accreditation
Diagnosis of non rare thrombophilia (F2, F5 genes)
Hopital Foch
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technical procedure(s) : PCR based techniques

GERMANY

Nordrhein-Westfalen
KÖLN

Accreditation
Molecular diagnosis of factor V Leiden mutation
laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing

GERMANY

Nordrhein-Westfalen
KÖLN

Accreditation
Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the SERPINE1 gene)
laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

GERMANY

Nordrhein-Westfalen
KÖLN

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

UNITED KINGDOM

Devon
EXETER

Accreditation
Molecular diagnosis of Congenital Factor V Deficiency (Leiden)
Royal Devon and Exeter Hospital - Wonford site
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Devon
EXETER

Accreditation
Molecular diagnosis of hyperprothrombinemia (Prothrombin 20210A mutation)
Royal Devon and Exeter Hospital - Wonford site
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Greater Manchester
MANCHESTER

Accreditation
Molecular diagnosis of thrombophilia by genotyping (Factor V Leiden and Prothrombin G20210A)
Central Manchester University Hospitals - Manchester Royal Infirmary
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
SINGEN /HTWL.

Accreditation
Molecular diagnosis of factor V Leiden mutation
Institut für Laboratoriumsmedizin und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
SINGEN /HTWL.

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Institut für Laboratoriumsmedizin und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
SINGEN /HTWL.

Accreditation
Molecular diagnosis of MTHFR gene variant C677T
Institut für Laboratoriumsmedizin und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
BAD OEYNHAUSEN

Accreditation
Molecular diagnosis of MTHFR gene variant C677T
Ruhr-Universität Bochum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
BAD OEYNHAUSEN

Accreditation
Molecular diagnosis of factor V Leiden mutation
Ruhr-Universität Bochum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Plzen
KLATOVY

Accreditation
Molecular diagnosis of non rare thrombophilia (G20210A variant of the F2 gene)
BioLab spol. s.r.o.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
BAD STEBEN

Accreditation
Molecular diagnosis of factor V Leiden mutation
Institut für angewandte Humangenetik und Onkogenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

AUSTRIA

WIEN
WIEN

Accreditation
Molecular diagnosis of non rare thrombophilia (MTHFR gene variant C677T, F2 gene, F5 gene)
Medizinische Universität Wien
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
HEIDELBERG

Accreditation
Molecular diagnosis of factor V Leiden mutation
Zentrallabor des Universitätsklinikums Heidelberg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
HEIDELBERG

Accreditation
Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Zentrallabor des Universitätsklinikums Heidelberg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SWITZERLAND

Suisse Romande
GENÈVE

Accreditation
Molecular diagnosis of Factor V Deficiency (Leiden)
Hôpitaux Universitaires de Genève HUG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

BRETAGNE
LORIENT

Accreditation
Diagnosis of non rare thrombophilia (F2 gene)
BIOLOR
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

BRETAGNE
LORIENT

Accreditation
Molecular diagnosis of resistance to activated protein C (F5 gene)
BIOLOR
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

CZECH REPUBLIC

South Bohemia
CESKE BUDEJOVICE

Accreditation
Molecular diagnosis of non rare thrombophilia (MTHFR, F5 and F2 genes)
Centrum lekarske genetiky s.r.o.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

South Moravia
BRNO

Accreditation
Molecular diagnosis of non rare thrombophilia (F2, F5 and CFTR genes)
Cytogenetic laboratory Brno,s.r.o.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation
Molecular diagnosis of thrombosis risks (F5, F2 genes)
CHU de Marseille - Hôpital de la Timone
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Molecular diagnosis of thrombosis risks (F2, F5 genes)
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technical procedure(s) : PCR based techniques

CZECH REPUBLIC

Plzen
PLZEN

Accreditation
Molecular diagnosis of non rare thrombophilia (MTHFR, F2 and F5 genes)
Genetika Plzen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

South Moravia
HODONIN

Accreditation
Molecular diagnosis of non rare thrombophilia (MTHFR, F2 and F5 genes)
Chemila, spol. s r.o.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
STUTTGART

Accreditation
Molecular diagnosis of thrombophilia (marker FV, FII, MTHFR, 4G/5G polymorphism in the promoter of the PAI1 gene)
Labor Prof. Dr. G. Enders MVZ
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

UNITED KINGDOM

Nottinghamshire
NOTTINGHAM

Accreditation
Molecular diagnosis of thrombophilia risk factors (multiplex analysis of the prothrombin 20210G>A and F5 c.1601G>A variants)
Queen's Medical Centre
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

CENTRE
CHAMBRAY-LES-TOURS

Accreditation
Molecular diagnosis of non rare thrombophilia (F2, F5 genes)
SELAS Arnaud-Biolys-Origet
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

MIDI-PYRENEES
TOULOUSE

Accreditation
Molecular diagnosis of non rare thrombophilia (F2 and F5 genes)
CHU de Toulouse - Hôpital Purpan
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

CANADA

Ontario
KINGSTON

Accreditation
Molecular Diagnosis of Familial Thrombosis (FVL, prothrombin, MTHFR targeted mutation analysis)
Kingston General Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Inherited Predisposition to Thrombophilia (Factor V Leiden, FII G20210A, MTHFR C677T)
Toronto General Hospital
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

CANADA

Terre-Neuve-et-Labrador
ST. JOHN'S

Accreditation
Molecular Diagnosis of Predisposition to Thrombophilia (FVL, F2 c.*97G>A)
Health Sciences Centre
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
PARIS

Molecular diagnosis of non rare thrombophilia (F5 gene: mutation G1691A; F2 gene: G20210A mutation; MTHFR gene: C677T mutation)
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing, PCR based techniques

FRANCE

ILE-DE-FRANCE
BOBIGNY

Molecular diagnosis of non rare thrombophilia (MTHFR, F2 and F5 genes)
CHU Paris Seine-Saint-Denis - Hôpital Avicenne
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

GERMANY

Berlin
BERLIN

Molecular diagnosis of thrombophilia (marker FV, FII, MTHFR, 4G/5G polymorphism in the promoter of the PAI1 gene)
Berlin-Potsdam MVZ GbR
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Aragón
ZARAGOZA

Diagnosis of non rare thrombophilia (F2, F5, MTHFR genes)
Hospital Universitario Miguel Servet
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technical procedure(s) : PCR based techniques

PORTUGAL

SUL
LISBOA

Analysis of thrombosis predisposition genetic factors (MTHFR C667T and A1298C, PAI-1 -675G>A; F5: 1691 G>A; F2: 20210 G>A)
Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

ESTONIA

Tartu
TARTU

Molecular diagnosis of hyperprothrombinemia (Prothrombin G20210A mutation)
Tartu University Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ESTONIA

Tartu
TARTU

Molecular diagnosis of factor V Leiden
Tartu University Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

PORTUGAL

NORTE
PORTO

Molecular diagnosis of congenital factor II deficiency (F2 gene: Target mutation analysis - single mutation, G20210A mutation)
CGC Genetics / Centro de Genética Clínica
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis

FRANCE

LORRAINE
EPINAL

Molecular genetics diagnosis ofnon rare thrombophilia (F2, F5 genes)
Analysis - Laboratoire Lefaure & Petit
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

GERMANY

Niedersachsen
OSNABRÜCK

Molecular diagnosis of factor V Leiden mutation
Praxis Dres. Gencik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Niedersachsen
OSNABRÜCK

Molecular diagnosis of MTHFR gene variant C677T
Praxis Dres. Gencik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Niedersachsen
OSNABRÜCK

Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the SERPINE1 gene)
Praxis Dres. Gencik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

NORWAY

Vestlandet
BERGEN

Molecular diagnosis of factor V Leiden (F5 gene)
Haukeland University Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Berlin
BERLIN

Molecular diagnosis of factor V Leiden mutation
Praxis für medizinische Genetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

GERMANY

Bayern
ERLANGEN

Molecular diagnosis of factor V Leiden mutation
Humangenetisches Institut am Universitätsklinikum Erlangen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
REGENSBURG

Molecular diagnosis of factor V Leiden mutation
Gemeinschaftspraxis Dr. Susanne Ebner und Dr. Susanne Markus
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Niedersachsen
HILDESHEIM

Molecular diagnosis of factor V Leiden mutation
Gemeinschaftspraxis Dres. Algermissen / Justus / Wilke / Graf
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

TURKEY

TURKEY
ISTANBUL

Molecular diagnosis of factor V Leiden
BURC Genetics Diagnostic Center
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Comunidad Valenciana
VALENCIA

Diagnosis of non rare thrombophilia (F2, F5 genes)
Hospital Universitario y Politécnico La Fe
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technical procedure(s) : PCR based techniques

GERMANY

Nordrhein-Westfalen
MÜNSTER

Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Institut für Humangenetik des Universitätsklinikums Münster
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
MÜNSTER

Molecular diagnosis of factor V Leiden mutation
Institut für Humangenetik des Universitätsklinikums Münster
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
REGENSBURG

Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Gemeinschaftspraxis Dr. Susanne Ebner und Dr. Susanne Markus
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

VENETO
COSTOZZA DI LONGARE

Molecular diagnosis of thrombophilia (F5 gene)
B.I.R.D. Foundation
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SWITZERLAND

Suisse Alémanique
REINACH

Molecular diagnosis of factor V deficiency and resistance to activated protein C (Leiden, R506Q mutation)
Diagene Laboratories Inc.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SWITZERLAND

Suisse Alémanique
REINACH

Molecular diagnosis of Homocystinuria due to Methylene Tetrahydrofolate Reductase deficiency (MTHFR gene: C677T mutation)
Diagene Laboratories Inc.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hessen
FRANKFURT AM MAIN

Molecular diagnosis of MTHFR gene variant C677T
bio.logis Zentrum für Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hessen
FRANKFURT AM MAIN

Molecular diagnosis of factor V Leiden mutation
bio.logis Zentrum für Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

LAZIO
ROMA

Molecular diagnosis of factor V Leiden mutation
Policlinico Umberto I
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hamburg
HAMBURG

Molecular diagnosis of factor V Leiden mutation
Pränatalzentrum Hamburg und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hamburg
HAMBURG

Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Pränatalzentrum Hamburg und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hamburg
HAMBURG

Molecular diagnosis of MTHFR gene variant C677T
Pränatalzentrum Hamburg und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
NÜRNBERG

Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Medizinisches Versorgungszentrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
NÜRNBERG

Molecular diagnosis of factor V Leiden mutation
Medizinisches Versorgungszentrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
NÜRNBERG

Molecular diagnosis of MTHFR gene variants C677T and A1298C
Medizinisches Versorgungszentrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Bayern
NÜRNBERG

Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the SERPINE1 gene)
Medizinisches Versorgungszentrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Andalucía
MÁLAGA

Diagnosis of resistance to activated protein C (F5 gene)
Genetaq
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing

FRANCE

ILE-DE-FRANCE
SAINT-MANDÉ

Molecular diagnosis of non rare thrombophilia (F2 (G20210A mutation), F5 (Leiden mutation) genes)
Hôpital d'Instruction des Armées Bégin
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

BELGIUM

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Molecular diagnosis of Non rare thrombophilia (Factor V Leiden - R506Q)
Universitair Ziekenhuis Brussel - UZBrussel
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

BELGIUM

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Molecular test for predisposition to thrombophilia (F2 gene - 20210G>A)
Universitair Ziekenhuis Brussel - UZBrussel
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

PORTUGAL

NORTE
PORTO

Molecular diagnosis of predisposition to thrombophilia (F5 gene: targeted mutation analysis - single mutation (R506Q))
CGC Genetics / Centro de Genética Clínica
Purpose(s) : Post-natal diagnosis, Somatic genetics, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis

FRANCE

FRANCHE-COMTE
BESANÇON

Molecular diagnosis of non rare thrombophilia (F5 and F2 genes)
EFS - Bourgogne/Franche-Comté
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

BRETAGNE
BREST

Molecular diagnosis of risk factors for thrombosis (F5 and F2 genes)
CHRU de Brest - Hôpital Morvan
Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

POLAND

Warszawa
WARSAW

FRANCE

BOURGOGNE
DIJON

Molecular diagnosis of non rare thrombophilia (F5, F2 MTHFR genes)
CHU de Dijon - Plateau technique de Biologie
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

POITOU-CHARENTES
POITIERS

Molecular diagnosis of non rare thrombophilia (F2, F5 genes)
CHU de Poitiers
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

RHONE-ALPES
SAINT-PRIEST-EN-JAREZ

Molecular diagnosis of non rare thrombophilia (F5 and F2 genes)
CHU de Saint-Etienne - Hôpital Nord
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

POLAND

Poznan
POZNAN

Molecular diagnosis of risk factors for thrombophilia (Leiden mutation in F5 gene; G20210A variant in F2 gene; C677T in MTHFR gene - RFLP analysis)
Centrum Genetyki Medycznej GENESIS
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
HEIDELBERG

Molecular diagnosis of resistance to activated protein C (factor V Leiden, factor V Cambridge)
Molekulargenetisches Labor der Gemeinschaftspraxis
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
HEIDELBERG

Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Molekulargenetisches Labor der Gemeinschaftspraxis
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
HEIDELBERG

Molecular diagnosis of MTHFR gene variant C677T
Molekulargenetisches Labor der Gemeinschaftspraxis
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
HEIDELBERG

Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the SERPINE1 gene)
Molekulargenetisches Labor der Gemeinschaftspraxis
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

LOMBARDIA
BUSTO ARSIZIO

Molecular diagnosis of thrombophilia risks (F5, F2 and MTHFR genes)
Toma Advanced Biomedical Assays S.p.A.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

TURKEY

TURKEY
ANKARA

Molecular diagnosis of non rare thrombophilia (Leiden mutation in the F5 gene; G20210A mutation in the F2 gene; MTHFR C677T polymorphism)
Intergen Genetics Center
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ALSACE
MULHOUSE

Molecular diagnosis of non rare thrombophilia (F5 and F2 genes)
CH de Mulhouse - Hôpital Emile Muller
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Molecular diagnosis of non rare thrombophilia (F2 and F5 genes)
CHU Paris Est - Hôpital Saint-Antoine
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

AUVERGNE
CLERMONT-FERRAND

Molecular diagnosis of non rare thrombophilia (F2, F5 and MTHFR genes)
Faculté de médecine de Clermont-Ferrand
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

LANGUEDOC-ROUSSILLON
MONTPELLIER

Molecular diagnosis of non rare thrombophilia (F2 and F5 genes)
CHRU de Montpellier - Hôpital Saint-Eloi
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ALSACE
STRASBOURG

Molecular diagnosis of non rare thrombophilia (F5, F2 and MTHFR genes)
CHU de Strasbourg - Hôpital de Hautepierre
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

LORRAINE
METZ

Molecular diagnosis of thrombophilia: factor V Leiden (gene F5 mutation G1691A) and factor II (gene F2 mutation G20210A)
CHR de Metz-Thionville
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

SPAIN

Andalucía
ARMILLA

ITALY

EMILIA ROMAGNA
PARMA

Molecular diagnosis of non rare trombophilia (F2, F5, MTHFR genes)
Azienda Ospedaliera Universitaria di Parma
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Comunidad Valenciana
PATERNA

Molecular diagnosis of non rare thrombophilia (F2, F5 and MTHFR genes)
Sistemas Genómicos S.L.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

LOMBARDIA
SAN FERMO DELLA BATTAGLIA

Molecular diagnosis of thrombophilia risks (F2, F5, MTHFR)
ASST Lariana - Ospedale S.Anna di Como
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

ITALY

SICILIA
CATANIA

Molecular diagnosis of thrombophilia (F2, F5, MTHFR genes)
CPSS - Centro Polidiagnostico Servizi Sanitari
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Comunidad Valenciana
PATERNA

Molecular diagnosis of susceptibility to non rare thrombophilia (F2, F5 and MTHFR genes)
IMEGEN - Instituto de Medicina Genómica
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
ULM

Molecular diagnosis of non rare thrombophilia (MTHFR gene variant C677T)
MVZ Humangenetik Ulm
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

TOSCANA
PISA

Postnatal molecular diagnosis of thrombophilia (F2, F5, MTHFR genes)
Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing

GERMANY

Bayern
REGENSBURG

Molecular diagnosis of non rare thrombophilia (gene variant C677T)
Gemeinschaftspraxis Dr. Susanne Ebner und Dr. Susanne Markus
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

LORRAINE
VANDOEUVRE-LÈS-NANCY

Molecular diagnosis of non rare thrombophilia (F5 gene : Leiden mutations ; F2 gene : G20210A mutation)
CHU de Nancy - Hôpital de Brabois
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

GERMANY

Sachsen
DRESDEN

Molecular diagnosis of thrombophilia (F2 gene: G20210A mutation)
Gemeinschaftspraxis für Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Sachsen
DRESDEN

Molecular diagnosis of factor V Leiden mutation
Gemeinschaftspraxis für Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Sachsen
DRESDEN

Molecular diagnosis of MTHFR gene variants C677T and A1298C
Gemeinschaftspraxis für Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

LAZIO
ROMA

Molecular diagnosis of non rare thrombophilia (F2, F5, MTHFR genes)
Azienda Ospedaliera S. Camillo-Forlanini - Ospedale San Camillo
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

TOSCANA
PRATO

Molecular diagnosis of non rare thrombophilia (F2, F5 genes)
USL4 - Nuovo Ospedale Santo Stefano
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

AQUITAINE
BORDEAUX

Molecular diagnosis of non rare thrombophilia (MTHFR gene)
CHU de Bordeaux-GH Pellegrin
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

CANADA

Québec
MONTRÉAL

Molecular diagnosis of Factor V Leiden thrombophillia (F5 gene: G1691A mutation by real-time PCR)
Centre hospitalier universitaire Sainte-Justine
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

CANADA

Québec
MONTRÉAL

Molecular diagnosis of prothrombine-related thrombophilia (mutation G20210A of F2 gene)
Centre hospitalier universitaire Sainte-Justine
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

AUSTRIA

WIEN
WIEN

Molecular diagnosis of factor V Leiden mutation
Medizinische Universität Wien
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Andalucía
MÁLAGA

Molecular diagnosis of non rare thrombophilia (F5, F2, MTHFR genes)
Genetaq
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

La Rioja
LOGROÑO

Diagnosis of non rare thrombophilia (MTHFR, F2, F5 genes / mutations C677T, G20210A, R506Q)
CIBIR - Centro de Investigación Biomédica de La Rioja
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing

CANADA

Québec
MONTRÉAL

Molecular diagnosis of non rare thrombophilia (MTHFR gene: C677T mutation)
Centre hospitalier universitaire Sainte-Justine
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

LOMBARDIA
CUSANO MILANINO

Molecular diagnosis of thrombophilia risks (F5, F2 and MTHFR genes)
Istituto Auxologico Italiano
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

POLAND

Warszawa
WARSAW

SPAIN

Cataluña
TERRASSA

Molecular diagnosis of non rare thrombophilia (F2, F5, MTHFR genes)
Consorci Sanitari de Terrassa
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

PORTUGAL

CENTRO
OEIRAS

Molecular diagnosis of non rare thrombophilia (F5 gene mutation R506Q)
Laboratório de Análises Clínicas Dr. Joaquim Chaves
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

PORTUGAL

CENTRO
OEIRAS

Analysis of thrombosis predisposition genetic factors (MTHFR: C667T e A1298C; F5: FV Leiden; F2: G20210A)
Laboratório de Análises Clínicas Dr. Joaquim Chaves
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

SPAIN

Comunidad Valenciana
SANT JOAN D'ALACANT

Molecular diagnosis of non rare thrombophilia (F5 gene: mut. G1691A; F2 gene: mut. G20210A; MTHFR gene: mut. C677T, mut. A1298C)
Centro Inmunológico de Alicante (CIALAB)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

PORTUGAL

ILHAS
FUNCHAL

Molecular diagnosis of non rare thrombophilia (F2 gene: Analysis of G20210A mutation by sequencing of the 3' region by qPCR)
Universidade da Madeira
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

SPAIN

Comunidad Valenciana
ALICANTE

Molecular diagnosis of non rare thrombophilia (F5 gene / mutation G1691A; F2 gene / mutation G20210A)
Instituto Bernabeu Biotech
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

SICILIA
AVOLA

Molecular diagnosis of non rare trombophilia (FII, FV, MTHFR genes)
Laboratori Campisi s.r.l.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

LAZIO
ROMA

Molecular diagnosis of non rare trombophilia (FII, FV, MTHFR genes)
Istituto CSS-Mendel
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Asturias
OVIEDO

Molecular diagnosis of susceptibility to non rare thrombophilia (F2, F5, F12, MTHFR genes / PCR, region sequencing)
IMOMA - Instituto de Medicina Oncológica y Molecular de Asturias
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

SPAIN

Cataluña
TARRAGONA

Molecular diagnosis of polycythemia vera (F2 gene / 20210A mutation detection; F5 gene / R506Q mutation detection; MTHFR gene / C677T and A1298C mutations detection)
Hospital Universitari de Tarragona Joan XXIII
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

ITALY

VENETO
LIMENA

Molecular diagnosis of non rare trombophilia (analysis of F2, F5, MTHFR genes determined by Real Time PCR)
RDI - RETE DIAGNOSTICA ITALIANA
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
BOULOGNE-BILLANCOURT

Molecular diagnosis of non rare thrombophilia (F2 and F5 genes)
CHU Paris IdF Ouest - Hôpital Ambroise Paré
Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

SPAIN

País Vasco
SAN SEBASTIÁN

Diagnosis of the susceptibility to non rare thrombophilia (F2, F5 and MTHFR genes)
DNA Data
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

POLAND

Gdansk
GDANSK

"Molecular diagnosis of non rare thrombophilia (Leiden mutation; G20210A mutation in F2 gene; MTHFR gene: C677T and A1298C)
INVICTA Sp. z o.o.
Purpose(s) : Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : NGS sequencing (except WES)

ITALY

LOMBARDIA
VARESE

Molecular diagnosis of non rare thrombophilia (F5 gene)
A.O.U. Ospedale di Circolo e Fondazione Macchi - Università dell'Insubria
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : NGS sequencing (except WES)

GERMANY

Baden-Württemberg
HEIDELBERG

Molecular diagnosis of thrombophilia (4G/5G polymorphism in the promoter of the PAI1 gene)
Zentrum für Kinder- und Jugendmedizin - Angelika-Lautenschläger-Klinik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
POISSY

Molecular diagnosis of non rare thrombophilia (MTHFR, F2 and F5 genes)
Centre hospitalier intercommunal Poissy-Saint-Germain-en-Laye
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

UNITED KINGDOM

Greater London
LONDON

Molecular diagnosis of Factor V Leiden mutation (G1691A mutation)
King's College Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

PAYS DE LA LOIRE
LE MANS

Phenotypic test of resistance to activated protein C
Centre Hospitalier du Mans
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

LORRAINE
VANDOEUVRE-LÈS-NANCY

Diagnosis of resistance to activated protein C
CHU de Nancy - Hôpital de Brabois
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

RHONE-ALPES
GRENOBLE

Molecular diagnosis of non rare thrombophilia (F5, F2, MTHFR genes)
CHU de Grenoble site Nord - Institut de biologie et de pathologie
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FINLAND

Finland
TURKU

Molecular diagnosis of factor V Leiden
Turku University Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Andalucía
GRANADA

Molecular Diagnosis of Hyperprothombinemia
Hospital Universitario Virgen de las Nieves
Purpose(s) : Post-natal diagnosis

GERMANY

Hessen
GIEßEN

Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Humangenetische Praxis Dr. Schmidt & Mautner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hessen
GIEßEN

Molecular diagnosis of factor V Leiden mutation
Humangenetische Praxis Dr. Schmidt & Mautner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hessen
GIEßEN

Molecular diagnosis of MTHFR gene variants C677T and A1298C
Humangenetische Praxis Dr. Schmidt & Mautner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

LOMBARDIA
LODI

Molecular diagnosis of resistance to activated protein C (F5 gene)
Azienda Ospedaliera della Provincia di Lodi
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hessen
FRANKFURT AM MAIN

Molecular diagnosis of factor V Leiden mutation
Praxis Dr. med. Ulrike Beudt
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hessen
FRANKFURT AM MAIN

Molecular diagnosis of MTHFR gene variant C677T
Praxis Dr. med. Ulrike Beudt
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Hessen
FRANKFURT AM MAIN

Risk calculation on molecular basis for thrombophilia (F2 gene: G20210A mutation)
Praxis Dr. med. Ulrike Beudt
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Moravia-Silesia
OSTRAVA

Molecular diagnosis of non rare thrombophilia (F5 and F2 genes)
CGB laboratory Ltd.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Usti nad Labem
USTI NAD LABEM

Molecular diagnosis of non rare thrombophilia (F2 gene: G20210A variant; F5 gene: Leiden mutation; MTHFR gene)
Masaryk hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SLOVENIA

SLOVENIA
LJUBLJANA

Molecular diagnosis of factor V Leiden thrombophilia (F5 gene)
University Medical Center Ljubljana
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

PUGLIA
LECCE

Molecular diagnosis of resistance to activated protein C
Presidio Ospedaliero "Vito Fazzi" - ASL LE
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

HUNGARY

Közép-Magyarország
BUDAPEST

Molecular diagnosis of resistance to activated protein C by melting point analysis of F5 gene
Semmelweis University Hospital - 2nd Department of Paediatrics
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

DENMARK

Fyn
ODENSE

Molecular diagnosis of resistance to activated protein C (RFLP analysis of F5 gene)
Amplexa Genetics A/S
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

DENMARK

Fyn
ODENSE

Molecular diagnosis of factor II deficiency (RFLP analysis of F2 gene)
Amplexa Genetics A/S
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

CALABRIA
REGGIO CALABRIA

Molecular diagnosis of resistance to activated protein C
Azienda Ospedaliera BMM
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
ARGENTEUIL

Molecular diagnosis of non rare thrombophilia (F2 and F5 genes)
Centre hospitalier Victor Dupouy
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

CROATIA

CROATIA
ZAGREB

Molecular diagnosis of Factor V Deficiency (Leiden)
Zagreb Clinical Hospital Center
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

LATVIA

LATVIA
RIGA

Molecular diagnosis of Factor V Deficiency (Leiden)
BMC - Biomedical Research centre
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SERBIA

Serbia
BELGRADE

Molecular diagnosis of Factor V Deficiency (Leiden)
Institute of Molecular Genetics and Genetic Engineering
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ISRAEL

ISRAEL
HAIFA

Molecular diagnosis of Thrombophilia (APCR, MTHFR, Prothrombin, Mutation analysis)
The Bnai Zion Medical Center, Technion-Rappaport Faculty of Medicine
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

ISRAEL

ISRAEL
JERUSALEM

Molecular diagnosis of Hypercoagulation (FV, Prothrombin, MTHFR, Mutation analysis)
Shaare Zedek Medical Center
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ROMANIA

CLUJ
CLUJ-NAPOCA

Molecular diagnosis of MTHFR deficiency (C677T, A1298C and G1793A/T mutations)
Spitalul Judetean Clinc de Urgenta Cluj
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ROMANIA

CLUJ
CLUJ-NAPOCA

Molecular diagnosis of hyperprothrombinemia (mutation G20210A of F2 gene)
Spitalul Judetean Clinc de Urgenta Cluj
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ROMANIA

CLUJ
CLUJ-NAPOCA

Molecular diagnosis of resistance to activated protein C (F5 Leiden mutation)
Spitalul Judetean Clinc de Urgenta Cluj
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

POLAND

Lodz
LODZ

Molecular diagnosis of resistance to activated protein C (F5 gene : Leiden mutation)
Centralny Szpital Kliniczny Uniwersytetu Medycznego w Lodzi
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SLOVENIA

SLOVENIA
LJUBLJANA

Molecular diagnosis of resistance to activated protein C (F5 gene: Leiden mutation)
University Medical Center Ljubljana
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
PARIS

Molecular diagnosis of thrombophilia (F2, F5 and MTHFR genes)
Groupe Hospitalier Paris Saint-Joseph
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

GERMANY

Hessen
GIEßEN

Molecular diagnosis of thrombophilia (SERPINE1 gene: 4G/5G polymorphism, 844 A/G)
Humangenetische Praxis Dr. Schmidt & Mautner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Capital City Prague
PRAHA

Molecular diagnosis of factor V deficiency (F5 gene)
Sanatorium PRONATAL
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Capital City Prague
PRAHA

Molecular diagnosis of non rare thrombophilia (F2 gene: G20210A mutation; F5 gene: Leiden mutation)
Sanatorium PRONATAL
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

BRETAGNE
QUIMPER

Molecular diagnosis of thrombosis risks (F5 gene: Leiden mutation; F2 and MTHFR genes)
CHI de Cornouaille
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ALSACE
COLMAR

Molecular diagnosis of thrombosis risks (F5 gene : R506Q mutation; F2 gene: G20210A mutation)
Hôpital Pasteur - Hôpitaux civils de Colmar
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

PROVENCE-ALPES-COTE D'AZUR
TOULON

Molecular diagnosis of thrombosis risks (F5 and F2 genes)
CHI Toulon La Seyne-sur-Mer - Hôpital Sainte Musse
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons
Technical procedure(s) : PCR based techniques

CZECH REPUBLIC

Hradec Kralove
HRADEC KRALOVE

Molecular diagnosis of resistance to activated protein C (F5 gene: Leiden mutation)
Medical Genetics Laboratory
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Hradec Kralove
HRADEC KRALOVE

Molecular diagnosis of hyperprothrombinemia (F2 gene: G20210A mutation)
Medical Genetics Laboratory
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Hradec Kralove
HRADEC KRALOVE

Molecular diagnosis of MTHFR thermolabile variant: C677T mutation
Medical Genetics Laboratory
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GREECE

ATTIKI
ATHENS

Molecular diagnosis of resistance to activated protein C (F5 gene mutations)
Mitera General, Maternity and Children's Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

LANGUEDOC-ROUSSILLON
NÎMES

Molecular diagnosis of non rare thrombophilia (F2 (G20210A polymorphism), F5 (Leiden mutation), F12 (C46T polymorphism), PROCR (mutation A6936G) genes)
CHU de Nîmes - Hôpital Caremeau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

CHAMPAGNE-ARDENNE
TROYES

Molecular diagnosis of resistance to activated protein C (F2, F5, MTHFR genes: Leiden mutation)
CH de Troyes - Hôpital des Hauts-Clos
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

CHAMPAGNE-ARDENNE
TROYES

Molecular diagnosis of hyperprothrombinemia (F2 gene)
CH de Troyes - Hôpital des Hauts-Clos
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

CHAMPAGNE-ARDENNE
TROYES

Molecular diagnosis of non rare thrombophilia (MTHFR gene variant)
CH de Troyes - Hôpital des Hauts-Clos
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
GARCHES

Molecular diagnosis of thrombophilia (gène MTHFR ; F5 gene: Leiden mutation; F2 gene: G20210A mutation search by PCR)
CHU Paris IdF Ouest - Hôpital Raymond Poincaré
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
MONTFERMEIL

Molecular diagnosis of thrombophilia risk factors (F5 gene: Leiden mutation; F2 gene: G20210 mutation ; PCR analysis)
GHI Le Raincy-Montfermeil
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

CENTRE
MONTARGIS

Molecular diagnosis of thrombophilia risks (F5 gene: Leiden mutation; F2 gene: G20210A mutation; real-time PCR analysis)
MEDIBIO
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
SAINT-DENIS

Molecular diagnosis of thrombophilia risk factors (F5 gene: Leiden mutation; F2 gene: G20210A mutation)
Centre Hospitalier de Saint-Denis
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

BELGIUM

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Molecular diagnosis of Predisposition to thrombophilia (specific F5 & F2 mutations)
Cliniques Universitaires UCL de Saint Luc - UCLStLuc
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics

FRANCE

PAYS DE LA LOIRE
LE MANS

Molecular diagnosis of thrombophilia (F5 gene: Leiden mutation; F2 gene: G20210A mutation; MTHFR gene)
Centre Hospitalier du Mans
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

SLOVENIA

SLOVENIA
MARIBOR

Molecular diagnosis of non rare thrombophilia
Maribor general hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

RHONE-ALPES
CHAMBERY

Molecular diagnosis of non rare thrombophilia (F2, F5 genes)
Hotel-Dieu
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

LIMOUSIN
LIMOGES

Molecular diagnosis of predisposition to thrombosis (F5, F2 and MTHFR genes)
CHU de Limoges - Hôpital Dupuytren
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing, PCR based techniques

FRANCE

ILE-DE-FRANCE
CORBEIL-ESSONNES

Molecular diagnosis of non rare thrombophilia (F5 gene: Leiden mutation; F2 gene; G20210A variant)
Centre Hospitalier Sud Francilien
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

POLAND

Kraków
KRAKOW

Molecular diagnosis of non rare thrombophilia (F2 gene: G20210A mutation; MTHFR gene: C677T variant)
Uniwersytecki Szpital Dzieciecy w Krakowie
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GREECE

IRAKLIO
HERAKLION

ITALY

LOMBARDIA
BRESCIA

Molecular diagnosis of thrombophilia (FII, FV and MTHFR genes)
Biodiversity
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

NORD-PAS-DE-CALAIS
LENS

Molecular diagnosis of non rare thrombophilia (F5 and F2 genes)
Centre hospitalier de Lens
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Molecular diagnosis of non rare thrombophilia
CHU Paris - Hôpital Necker-Enfants Malades
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

CZECH REPUBLIC

Capital City Prague
PRAHA

Molecular diagnosis of non rare thrombophilia (F5 gene: Leiden mutation; F2: G20210A variant; MTHFR gene)
Gennet s.r.o.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

AQUITAINE
BORDEAUX

Molecular diagnosis of non rare thrombophilia (F5, F2 genes)
CHU de Bordeaux-GH Pellegrin
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

RHONE-ALPES
LYON

Molecular diagnosis of non rare thrombophilia (F5, F2 and MTHFR genes)
Centre de Biologie et de Pathologie Est
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

CENTRE
TOURS

Molecular diagnosis of non rare thrombophilia (F2 and F5 genes)
CHRU de Tours - Hôpital Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Molecular diagnosis of thrombosis risks (F2, F5 and MTHFR genes)
CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

BASSE-NORMANDIE
CAEN

Molecular diagnosis of thrombosis risks (F5 and F2 genes)
CHU de Caen - Hôpital de la Côte de Nacre
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Molecular diagnosis of thrombosis risks (F5 and F2 genes)
CHU Paris IdF Ouest - HEGP Hôpital Européen Georges Pompidou
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

ISRAEL

ISRAEL
TEL AVIV

Molecular diagnosis of non rare thrombophilia (F5, F2 and MTHFR genes)
Pronto Diagnostics Ltd.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

CALABRIA
MANGONE

Molecular diagnosis of risk factors for thrombophilia (F2, F5, MTHFR genes)
CNR
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Capital City Prague
PRAHA

Molecular diagnosis of non rare thrombophilia (MTHFR, F2 and F5 genes)
IHBT - Institute of hematology and blood transfusion
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Olomouc
OLOMOUC

Molecular diagnosis of non rare thrombophilia (F5, F2 and MTHFR genes)
University hospital Olomouc
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
LE KREMLIN-BICÊTRE

Molecular diagnosis of non rare thrombophilia (F2 and F5 genes)
GHU Paris-Sud - Hôpital de Bicêtre
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Molecular diagnosis of non rare thrombophilia (F2, F5 and MTHFR genes)
CHU Paris - Hôpital Robert Debré
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Molecular diagnosis of non rare thrombophilia (F2 et F5 genes)
CHU Paris Centre - Hôpital Cochin
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

PICARDIE
AMIENS

Molecular diagnosis of non rare thrombophilia (F2, F5 genes and C677T , A1298C mutations in MTHFR gene)
CHU Amiens-Picardie - Site Sud
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Molecular diagnosis of non rare thrombophilia (F5 (Leiden mutation and HR2 haplotype), F2 and MTHFR genes)
CHU Paris-GH St-Louis Lariboisière F.Widal - Hôpital Lariboisière
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

CHAMPAGNE-ARDENNE
REIMS

Molecular diagnosis of non rare thrombophilia (Leiden mutation in the F5 gene, MTHFR gene and G20210A variant in the F2 gene)
CHU de Reims - Hôpital Robert Debré
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

HAUTE-NORMANDIE
ROUEN

Molecular diagnosis of non rare thrombophilia (F5, F and MTHFR genes)
CHU de Rouen - Hôpital Charles Nicolle
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
CRÉTEIL

Molecular diagnosis of non rare thrombophilia (F5 gene: Leiden mutation; F2 gene: G20210A variant)
CHU Henri Mondor
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of susceptibility to non rare thrombophilia (F5 and F2 genes)
CHU Paris Est - Hôpital Tenon
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Uniparental disomy study, Deletion / Duplication analysis
Technical procedure(s) : PCR based techniques

CZECH REPUBLIC

South Bohemia
CESKE BUDEJOVICE

Molecular diagnosis of non rare thrombophilia (MTHFR, F2 and F5 genes)
Hospital Ceské Budejovice
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Liberec
LIBEREC

Molecular diagnosis of non rare thrombophilia (MTHFR, F2 and F5 genes)
Regional Hospital Liberec, Krajska nemocnice Liberec
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Plzen
PLZEN

Molecular diagnosis of non rare thrombophilia (MTHFR, F2 and F5 genes)
Genomia s.r.o.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Capital City Prague
PRAHA

Molecular diagnosis of non rare thrombophilia (MTHFR gene; F2 gene: G21210A variant; F5 gene: G1691A mutation)
GENvia Genetic Laboratory Ltd.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
AULNAY-SOUS-BOIS

Molecular diagnosis of non rare thrombophilia (F2 and F5 gene)
Centre Hospitalier Robert Ballanger
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

AQUITAINE
VILLENAVE D'ORNON

Molecular diagnosis of non rare thrombophilia (F2 and F5 Leiden genes)
Hôpital d'Instruction des Armées Robert PICQUE
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

SPAIN

La Rioja
LOGROÑO

Molecular diagnosis of non rare thrombophilia (F2, F5 and MTHFR genes)
Hospital San Pedro
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

SICILIA
MESSINA

Molecular diagnosis of thrombophilia (F2, F5, MTHFR genes)
A.O.U. Policlinico "G. Martino"
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

SARDEGNA
OZIERI

Molecular diagnosis of thrombophilia (F2, F5, MTHFR genes)
Presidio Ospedaliero di Ozieri - ASL 1
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Madrid
MAJADAHONDA

Molecular diagnosis of non rare thrombophilia (F5 and MTHFR genes)
Genyca Innova
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

LAZIO
ROMA

Molecular diagnosis of non rare thrombophilia (F2, F5, MTHFR genes)
USI - Unione Sanitaria Internazionale
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CANADA

Québec
QUÉBEC

Molecular diagnosis of non rare thrombophilia (F5 gene / mutation G1691A)
CHUQ - Centre Hospitalier Universitaire de Québec - Hôtel-Dieu de Québec
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CANADA

Québec
QUÉBEC

Molecular diagnosis of non rare thrombophilia (F2 gene / mutation G20210A)
CHUQ - Centre Hospitalier Universitaire de Québec - Hôtel-Dieu de Québec
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Andalucía
CÁDIZ

Molecular diagnosis of non rare thrombophilia (F5, F2, MTHFR genes)
Hospital Universitario Puerta del Mar
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

LATVIA

LATVIA
RIGA

Molecular diagnosis of non rare thrombophilia (F5, F2 and MTHFR gene: search for specific mutations)
Riga Stradins University
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SLOVAKIA

Bratislavsky kraj
BRATISLAVA

Molecular diagnosis of hereditary thrombophilia (F5 gene: G1591A and H1299R; F2 gene: G20210A; MTHFR gene: C677T and A1298C; PROCR gene: A4600G and G4678C)
University Hospital Bratislava - Stare mesto
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

POLAND

Lodz
LODZ

Molecular diagnosis of non rare thrombophilia (F5 gene: Leiden mutation; F2 gene: G20210A variant; MTHFR gene: C677T and A1298C variants)
Centralny Szpital Kliniczny
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

BRETAGNE
RENNES

Molecular diagnosis of non rare thrombophilia (F2, F5 genes)
CHU de Rennes - Hôpital Pontchaillou
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

UNITED KINGDOM

Oxfordshire
OXFORD

Molecular diagnosis of Thrombophilia (F5, F2 genes)
John Radcliffe Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

MOLISE
POZZILLI

Molecular diagnosis of non rare trombophilia (FII, FV, MTHFR genes)
Istituto Neurologico Mediterraneo - IRCCS Neuromed
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing, PCR based techniques

MOROCCO

Rabat
RABAT

Molecular diagnosis of factor V Leiden mutation
Institut National d'Hygiène
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

BASILICATA
MATERA

Postnatal molecular diagnosis of non rare trombophilia (FV, FII, MTHFR genes)
Presidio Ospedaliero "Madonna delle Grazie" - Azienda Sanitaria di Matera (ASM)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

PAYS DE LA LOIRE
NANTES

Molecular diagnosis of non rare thrombophilia (F2, F5 genes)
CHU de Nantes - Institut de Biologie
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
GONESSE

Molecular diagnosis of non rare thrombophilia (F5 gene: mutation G1691A; F2 gene: G20210A mutation; MTHFR gene: C677T mutation)
Centre Hospitalier de Gonesse
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of major susceptibility factor in non rare thrombophilia (F5 gene: mutation screening in G1691A; F2 gene: mutation screening in G20210A; MTHFR gene: mutation screening in C677T and A1298C; F12 gene/polymorphism screening in C46T)
Laboratorio de Genética Clínica, S.L.
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

FRANCE

CENTRE
ORLEANS

Molecular diagnosis of thrombosis risks (F2: G20210A mutation, F5: Leiden mutation and MTHFR genes)
CHR d'Orléans - Hôpital de la Source
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques