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GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene: sequencing, MLPA)
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
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

Hamburg
HAMBURG

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene)
Labor Lademannbogen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Sachsen
WEIßWASSER

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene: sequencing)
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

Greater London
LONDON

Accreditation
Molecular diagnosis of Protein C deficiency (PROC gene)
St Thomas' Hospital
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technical procedure(s) : Sanger sequencing, MLPA based techniques

SPAIN

Cataluña
BARCELONA

Accreditation
Molecular Diagnosis of Thrombophilia due to Protein C Deficiency
Laboratorio de Análisis Dr. Echevarne
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

South Yorkshire
SHEFFIELD

Accreditation
Molecular diagnosis of Protein C deficiency (PROC gene)
Sheffield Children's NHS Foundation Trust
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene)
Centogene AG
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 protein C deficiency (PROC gene)
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
LEIPZIG

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene)
MVZ Labor Dr. Reising-Ackermann und Kollegen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene: sequencing / MLPA)
Diagenom GmbH
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
MANNHEIM

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene)
Zentrum für Humangenetik Mannheim
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 protein C deficiency (PROC gene: sequencing)
Mitteldeutscher Praxisverbund Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Niedersachsen
HANNOVER

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene)
amedes genetics im MVZ wagnerstibbe
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Nordrhein-Westfalen
DUISBURG

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene: sequencing / MLPA)
Gerinnungszentrum Rhein-Ruhr
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

Bayern
MARTINSRIED

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene)
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

SWITZERLAND

Suisse Romande
GENÈVE

Accreditation
Diagnosis of congenital protein C deficiency (protein C dosage)
Hôpitaux Universitaires de Genève HUG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

GERMANY

Bayern
MÜNCHEN

Accreditation
Molecular diagnosis of rare hereditary thrombophilia (HCF2, HRG, PROC, PROS1, PLAT, F9 genes)
Pränatalmedizin München
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technical procedure(s) : Sanger sequencing, MLPA based techniques

NETHERLANDS

Gelderland
NIJMEGEN

Accreditation
Molecular diagnosis of Thrombophilia due to Protein C Deficiency (PROC gene)
Radboudumc - Radboud universitair medisch centrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of hereditary thrombophilia due to congenital protein C deficiency (PROC gene)
Reference Laboratory Genetics
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 protein C deficiency (PROC 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) : Sanger sequencing

FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation
Diagnosis of congenital protein C deficiency
CHU de Marseille - Hôpital de la Timone
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

NORD-PAS-DE-CALAIS
LILLE

Accreditation
Diagnosis of congenital protein C deficiency
CHRU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
LE KREMLIN-BICÊTRE

Accreditation
Diagnosis of congenital protein C deficiency (biological phenotype)
GHU Paris-Sud - Hôpital de Bicêtre
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of congenital protein C deficiency
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

CENTRE
TOURS

Accreditation
Diagnosis of congenital protein C deficiency
CHRU de Tours - Hôpital Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

AUSTRIA

WIEN
WIEN

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene)
Medizinische Universität Wien
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
BONN

Accreditation
Molecular diagnosis of protein C deficiency (PROC gene)
Universitätsklinikum Bonn
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

IRELAND

County Dublin
DUBLIN

Accreditation
Molecular diagnosis of Protein C deficiency (PROC gene)
St James's Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technical procedure(s) : NGS sequencing (except WES)

UNITED KINGDOM

West Midlands
BIRMINGHAM

Accreditation
Molecular diagnosis of Protein C deficiency (PROC gene)
Birmingham Children's Hospital NHS Foundation Trust
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Nottinghamshire
NOTTINGHAM

Accreditation
Molecular diagnosis of Protein C deficiency (PROC gene)
Queen's Medical Centre
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

FRANCE

HAUTE-NORMANDIE
ROUEN

Accreditation
Molecular diagnosis of hereditary thrombophilia due to congenital protein C deficiency (PROC gene)
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

UNITED KINGDOM

Devon
EXETER

Accreditation
Molecular diagnosis of Thrombophilia Due To Activated Protein C Resistance (diagnosis by targetted mutation analysis) (F5 gene)
Royal Devon and Exeter Hospital - Wonford site
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

FRANCE

LANGUEDOC-ROUSSILLON
MONTPELLIER

Diagnosis of congenital protein C deficiency
CHRU de Montpellier - Hôpital Saint-Eloi
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

MIDI-PYRENEES
TOULOUSE

Diagnosis of congenital protein C deficiency
CHU de Toulouse - Hôpital Purpan
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

GERMANY

Hamburg
HAMBURG

Molecular diagnosis of protein C deficiency (PROC gene)
Pränatalzentrum Hamburg und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Baden-Württemberg
HEIDELBERG

Molecular diagnosis of protein C deficiency (PROC gene: sequencing)
Molekulargenetisches Labor der Gemeinschaftspraxis
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

PORTUGAL

SUL
LISBOA

Molecular diagnosis of protein C deficiency (PROC gene): sequence analysis of the entire coding region
Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region

GERMANY

Nordrhein-Westfalen
BONN

Molecular diagnosis of protein C deficiency (PROC gene)
Institut für Klinische Genetik Bonn
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

PORTUGAL

CENTRO
COIMBRA

Molecular diagnosis of congenital protein C deficiency (PROC gene): sequencing of the entire coding region and deletion/duplication analysis
Hosp. Pediátrico e Hosp. Covões - Centro Hospitalar e Universitário de Coimbra
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis

GERMANY

Sachsen
DRESDEN

Molecular diagnosis of protein C deficiency (PROC gene: sequencing / MLPA)
Gemeinschaftspraxis für Humangenetik
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

CANADA

Québec
MONTRÉAL

Molecular diagnosis of Hereditary thrombophilia due to congenital protein C deficiency (PROC gene / mutation 3363insC)
Centre hospitalier universitaire Sainte-Justine
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

PORTUGAL

NORTE
PORTO

Molecular diagnosis of protein C deficiency (PROC gene: sequencing of the entire coding region)
CGC Genetics / Centro de Genética Clínica
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region

SPAIN

Comunidad Valenciana
PATERNA

Molecular diagnosis of hereditary thrombophilia due to congenital protein C deficiency (PROC gene)
IMEGEN - Instituto de Medicina Genómica
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Andalucía
MÁLAGA

Molecular diagnosis of hereditary thrombophilia due to congenital protein C deficiency (PROC gene)
Genetaq
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
STUTTGART

Molecular diagnosis of protein C deficiency (PROC gene)
Praxis für Humangenetik und Prävention
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

SPAIN

Comunidad Valenciana
ELCHE

Diagnosis of hereditary thrombophilia due to congenital protein C deficiency (PROC gene)
Bioarray
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : NGS sequencing (except WES)

HUNGARY

Észak-Magyarország
DEBRECEN

Molecular diagnosis of protein C deficiency (PROC gene)
University of Debrecen
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

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis and characterisation of genetic anomalies of protein C (PROC gene)
CHU Paris IdF Ouest - HEGP Hôpital Européen Georges Pompidou
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

FRANCE

PAYS DE LA LOIRE
LE MANS

Diagnosis of congenital protein C deficiency
Centre Hospitalier du Mans
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
BONDY

Diagnosis of congenital protein C deficiency
CHU Paris Seine-Saint-Denis - Hôpital Jean Verdier
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

PICARDIE
AMIENS

Diagnosis of congenital protein C deficiency
CHU Amiens-Picardie - Site Sud
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

BRETAGNE
RENNES

Diagnosis of congenital protein C deficiency
CHU de Rennes - Hôpital Pontchaillou
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ALSACE
MULHOUSE

Diagnosis of congenital protein C deficiency
CH de Mulhouse - Hôpital Emile Muller
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

MIDI-PYRENEES
TOULOUSE

Diagnosis of congenital protein C deficiency
CHU de Toulouse - Hôpital Rangueil
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of congenital protein C deficiency (activity measurement)
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of congenital protein C deficiency
CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of congenital protein C deficiency
CHU Paris Centre - Hôpital Cochin
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of congenital protein C deficiency
CHU Paris - Hôpital Robert Debré
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

LORRAINE
VANDOEUVRE-LÈS-NANCY

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

FRANCE

AUVERGNE
CLERMONT-FERRAND

Diagnosis of congenital protein C deficiency
CHU de Clermont-Ferrand - Hôpital d'Estaing
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

ITALY

PUGLIA
SAN GIOVANNI ROTONDO

Molecular and biochemical diagnosis of protein C deficiency (PROC gene)
IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Biochemical genetics
Objective(s) : Analyte / Enzyme assay

FRANCE

ILE-DE-FRANCE
ARGENTEUIL

Diagnosis of congenital deficiency of coagulation factors
Centre hospitalier Victor Dupouy
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
ARGENTEUIL

Diagnosis of congenital protein C deficiency (chronometric assay)
Centre hospitalier Victor Dupouy
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

AQUITAINE
BORDEAUX

Molecular diagnosis of congenital protein C deficiency
CHU de Bordeaux-GH Pellegrin
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Deletion / Duplication analysis
Technical procedure(s) : Sanger sequencing, MLPA based techniques

SPAIN

Comunidad Valenciana
ALICANTE

Molecular diagnosis of Protein C Deficiency. Thrombotic Disease.
Análisis Genéticos ANCOR S.L.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SERBIA

Serbia
BELGRADE

Diagnosis of inherited bleeding disorders (hemophilia, von Willebrand disease and others rare bleeding disorders)
Blood Transfusion Institute of Serbia
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

ILE-DE-FRANCE
MEAUX

Diagnosis of congenital protein C deficiency
CH de l'Est Francilien, site de Meaux
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

CZECH REPUBLIC

Capital City Prague
PRAHA

Molecular diagnosis of hereditary thrombophilia due to congenital protein C deficiency (PROC gene)
IHBT - Institute of hematology and blood transfusion
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Oxfordshire
OXFORD

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

UNITED KINGDOM

Greater London
LONDON

Molecular diagnosis of Thrombophilia Due To Activated Protein C Resistance (F2, F5 genes: Targetted mutation analysis)
King's College Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
BOBIGNY

Diagnosis of congenital protein C deficiency
CHU Paris Seine-Saint-Denis - Hôpital Avicenne
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of hereditary thrombophilia due to congenital protein C deficiency (PROC gene)
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, Deletion / Duplication analysis
Technical procedure(s) : Sanger sequencing, MLPA based techniques