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GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Molecular diagnosis of myeloproliferative disorders (JAK2(V617F), MPL, TET2 genes)
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

GERMANY

Niedersachsen
HANNOVER

Accreditation
Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene: V617F)
Medizinische Hochschule Hannover
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : Sanger sequencing

GERMANY

Rheinland-Pfalz
INGELHEIM AM RHEIN

Accreditation
Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene: mutation V617F)
Bioscientia Institut für Medizinische Diagnostik GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GREECE

ATTIKI
ATHENS

Accreditation
Molecular diagnosis of myeloproliferative diseases : search for V617F mutation in JAK2 gene by ARMS-PCR
BioAnalytica-GenoType SA
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

UNITED KINGDOM

South Yorkshire
SHEFFIELD

Accreditation
Molecular diagnosis of chronic myeloproliferative diseases (JAK2: by mutation analysis for V617F)
Sheffield Children's NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

UNITED KINGDOM

South Yorkshire
SHEFFIELD

Accreditation
Molecular monitoring of donor chimerism post stem cell transplantation
Sheffield Children's NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

NORD-PAS-DE-CALAIS
VALENCIENNES

Accreditation
Molecular diagnosis of malignant haemopathies
Centre Hospitalier de Valenciennes
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

NORD-PAS-DE-CALAIS
VALENCIENNES

Accreditation
Cytogenetic diagnosis of malignant haemopathies
Centre Hospitalier de Valenciennes
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics

GERMANY

Berlin
BERLIN

Accreditation
Molecular cytogenetic diagnosis of chronic myeloproliferative disease
Charité - Universitätsmedizin Berlin (CVK)
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technical procedure(s) : FISH

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation
Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene: mutation V617F)
Diagenom GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation
Cytogenetic/ molecular cytogenetic diagnosis of chronic myeloproliferative disorders
Diagenom GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technical procedure(s) : FISH

FRANCE

ILE-DE-FRANCE
SAINT-OUEN-L'AUMÔNE

Accreditation
Molecular diagnosis of myeloproliferative syndromes (V617F mutation in JAK2 gene)
Laboratoire Cerba
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GERMANY

Hamburg
HAMBURG

Accreditation
Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene: V617F)
Labor Lademannbogen
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation
Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene: sequencing / MLPA)
Centogene AG
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technical procedure(s) : Sanger sequencing, MLPA based techniques

UNITED KINGDOM

Avon
BRISTOL

Accreditation
Molecular haemato-oncology diagnosis of myeloproliferative syndromes (JAK2 gene: V617F mutation and exon 12 analysis)
Southmead Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GERMANY

Sachsen
DRESDEN

Accreditation
Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene)
Mitteldeutscher Praxisverbund Humangenetik
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

SWITZERLAND

Suisse Romande
SION

Accreditation
Molecular diagnosis of myeloproliferative syndromes (V617F mutation in JAK2 gene)
Institut Central des Hôpitaux Valaisans (ICHV)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Molecular diagnosis of chromosomal aberrations in AML, ALL, CML, AUL, CMML, MPN
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

West Midlands
BIRMINGHAM

Accreditation
Molecular diagnosis of myeloproliferative disorders (JAK2 gene: V617 mutation)
Birmingham Women's NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Avon
BRISTOL

Accreditation
Molecular diagnosis of Chronic myeloproliferative disease (MPL gene)
Southmead Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Wiltshire
SALISBURY

Accreditation
Molecular diagnosis of Myeloproliferative disorders (JAK2 gene:mutation V617F: ARMSPCR and pyrosequencing, 9q24)
Salisbury District Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

GERMANY

Baden-Württemberg
TÜBINGEN

Accreditation
Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene)
CeGaT GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technical procedure(s) : Sanger sequencing, MLPA based techniques

GERMANY

Nordrhein-Westfalen
KÖLN

Accreditation
Molecular cytogenetic diagnosis of essential thrombocythemia (CEP8 (8p11.1-q11.1), Chr.9: abl (9q34), Chr. 13: D13S319 (13q14.3)/ 13q34, TP53 (17p13.1), D20S108 (20q12))
Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technical procedure(s) : FISH

GERMANY

Hamburg
HAMBURG

Accreditation
Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene)
MVZ Fenner & Krasemann
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

ITALY

VENETO
PADOVA

Accreditation
Molecular diagnosis of myeloproliferative diseases (JAK2 gene)
Azienda Ospedaliera di Padova
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

BELGIUM

LIEGE
LIEGE

Accreditation
Molecular diagnosis of essential thrombocythemia and primary myelofibrosis (CALR gene)
CHU de LIEGE - UniLab Lg
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

CANADA

Ontario
MISSISSAUGA

Accreditation
Molecular Diagnosis of Myeloproliferative Disorder (JAK2 targeted mutation analysis)
Trillium Health Partners- Credit Valley Site
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

SWITZERLAND

Suisse Romande
GENÈVE

Accreditation
Conventional (karyotype) and molecular cytogenetics (FISH) diagnosis of myeloproliferative neoplasm: diagnosis and prognosis
Hôpitaux Universitaires de Genève HUG
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technical procedure(s) : FISH, Karyotyping

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of essential thrombocythemia (CALR, JAK2, MPL genes)
Reference Laboratory Genetics
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

ILE-DE-FRANCE
PARIS

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

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular diagnosis of myeloproliferative disorders (JAK2 (exon 12, exon 14 (V617F)), MPL (exon 10), TET2 (exon 3-11) and PRV1 genes)
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

UNITED KINGDOM

Devon
EXETER

Accreditation
Molecular diagnosis of myeloproliferative disorders (JAK2 gene)
Royal Devon and Exeter Hospital - Wonford site
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
ULM

Accreditation
Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene)
DRK Baden-Württemberg/ Hessen
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

SWEDEN

Landstinget i Östergötland
LINKÖPING

Accreditation
Molecular diagnosis of myeloproliferative disorders (JAK2 gene)
Universitetssjukhuset i Linköping
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular cytogenetic and cytogenetic diagnosis of chronic myeloproliferative disorders (translocations: t(3q26) [EVI1] deletions: 4q24 [TET2], 5q31 [EGR1] / 5q33-q34 [CSF1R], 7q22.1/7q31 [RELN/TES], 17p13 [TP53], 20q12 [MYBL2] numeric: -7 [RELN/TES], +8 [cen8], -Y [cen Y])
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technical procedure(s) : FISH

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular cytogenetic and cytogenetic diagnosis of myeloproliferative disorders (translocations: t(9;22) [BCR/ABL1], t(5q31-q33) [PDGFRB], deletions: 4q24 [TET2], 20q12 [MYBL2] numeric: +8 [cen8]
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technical procedure(s) : FISH

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular diagnosis of chronic myeloproliferative disorders (TET2 gene (exon 3-11), JAK2 gene (V617F), TP53 (exon 4-9))
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technical procedure(s) : Sanger sequencing

AUSTRIA

WIEN
WIEN

Accreditation
Molecular diagnosis of essential thrombocythemia (V617F mutation of the JAK2 gene)
Medizinische Universität Wien
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

CENTRE
CHAMBRAY-LES-TOURS

Accreditation
Molecular diagnosis of myeloproliferative disorders (JAK2 gene)
SELAS Arnaud-Biolys-Origet
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Myeloproliferative Disorder (JAK2 V617F, CALR targeted mutation analysis)
Toronto General Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

CANADA

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

Accreditation
Molecular Diagnosis of Myeloproliferative Disorder (JAK2 V617F mutation analysis)
Health Sciences Centre
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

CANADA

Ontario
LONDON

Accreditation
Molecular Diagnosis of Myeloproliferative Disorder (JAK2 V617F targeted mutation analysis)
London Health Sciences Centre
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

CANADA

Ontario
HAMILTON

Accreditation
Molecular Diagnosis of Myeloproliferative Neoplams (JAK2 exon 12, V617F, MPL515 targeted mutation)
McMaster University Medical Centre
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons
Technical procedure(s) : PCR based techniques

FRANCE

LANGUEDOC-ROUSSILLON
MONTPELLIER

Cytogenetic diagnosis of malignant hemopathies
CHRU de Montpellier - Hôpital Saint-Eloi
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics

GREECE

THESSALONIKI
THESSALONIKI

Molecular cytogenetics diagnosis of myeloproliferative diseases
Theagenion Cancer Centre of Thessaloniki
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics

TURKEY

TURKEY
ISTANBUL

Molecular diagnosis of myeloproliferative disorder with oesinophilia (PDGFRB gene)
Genetiks - Genetic diagnosis and research center
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

TURKEY

TURKEY
ISTANBUL

Molecular diagnosis of chronic myeloproliferative syndromes (JAK2 gene)
Genetiks - Genetic diagnosis and research center
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
SAINT-MANDÉ

Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene)
Hôpital d'Instruction des Armées Bégin
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

BRETAGNE
BREST

Molecular diagnosis of myeloproliferative syndromes (JAK2 gene: V617F mutation and exon 12 analysis)
CHRU de Brest - Hôpital Morvan
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

LORRAINE
METZ

Molecular diagnosis of myeloproliferative diseases (JAK gene: V617F mutation)
CHR de Metz-Thionville
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

LORRAINE
METZ

FISH diagnosis of hemopathies
CHR de Metz-Thionville
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technical procedure(s) : FISH

PORTUGAL

NORTE
PORTO

Molecular cytogenetic diagnosis of malignant haemopathies
Instituto Português de Oncologia do Porto, EPE / IPOFG - CRO Porto
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

SPAIN

País Vasco
SAN SEBASTIÁN

Molecular diagnosis of essential thrombocythemia (JAK2 gene / mutation V617F/G1849T)
Hospital Universitario Donostia
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

PORTUGAL

CENTRO
COIMBRA

Molecular diagnosis of Polycythaemia Vera, Essential Thrombocythaemia and Idiopathic Myelofibrosis (JAK2 gene): V617F mutation and exon 14 quantification (RT-PCR).
Hosp. Pediátrico e Hosp. Covões - Centro Hospitalar e Universitário de Coimbra
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

ITALY

LOMBARDIA
MILANO

Molecular cytogenetic and cytogenetic diagnosis of myeloproliferative neoplasias
Azienda Ospedaliera "San Paolo" - Università degli Studi di Milano
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technical procedure(s) : Karyotyping

POLAND

Bydgoszcz
BYDGOSZCZ

Molecular diagnosis of myeloproliferative syndromes (V617F mutation in JAK2 gene)
Szpital Uniwersytecki im. dr. Antoniego Jurasza
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

ITALY

FRIULI VENEZIA GIULIA
UDINE

Molecular diagnosis of thrombocythemia (JAK2, MPL genes)
Azienda Ospedaliero-Universitaria "Santa Maria della Misericordia" di Udine
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

SPAIN

Comunidad Valenciana
SANT JOAN D'ALACANT

Molecular cytogenetics diagnosis of essential thrombocythemia (FISH t(9;22), JAK2 gene: mut. V617F, exon 12; MPL gene: codon 505, 515)
Centro Inmunológico de Alicante (CIALAB)
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technical procedure(s) : FISH

SPAIN

Comunidad Valenciana
VALENCIA

Molecular diagnosis of chronic myeloproliferative diseases (JAK2 gene / PCR)
Hospital Universitario y Politécnico La Fe
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

SPAIN

Comunidad Valenciana
VALENCIA

Molecular diagnosis of myelodysplastic syndromes and myeloid hemopathy (TET2 gene / PCR)
Hospital Universitario y Politécnico La Fe
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

SPAIN

Andalucía
MÁLAGA

Molecular diagnosis of myeloproliferative disorders (MPL gene)
Genetaq
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Asturias
OVIEDO

Molecular cytogenetic diagnosis of myeloproliferative neoplasm (FISH)
Hospital Universitario Central de Asturias
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Technical procedure(s) : FISH

FRANCE

ALSACE
STRASBOURG

Cytogenetic diagnosis of myeloid hemopathies (classical caryotype and FISH)
CHU de Strasbourg - Hôpital de Hautepierre
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technical procedure(s) : FISH

FRANCE

FRANCHE-COMTE
BESANÇON

Molecular cytogenetic diagnosis of malignant hemopathies
CHRU de Besançon - Hôpital Saint-Jacques
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics

FRANCE

MIDI-PYRENEES
TOULOUSE

Cytogenetic diagnosis of myeloid hemopathies
CHU de Toulouse - Hôpital Purpan
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

Molecular and molecular cytogenetic diagnosis of Myeloproliferative neoplasm (BCR/ABL1, JAK2 (V617F and exon 12 mut), MPL (S505 and W515 mut), FIP1L1/PDGFRA
Cambridge University Hospitals NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics

GERMANY

Baden-Württemberg
STUTTGART

Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene)
Klinikum Stuttgart - Standort Olgahospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

FRANCE

AQUITAINE
PESSAC

Molecular and cytogenetic diagnosis of chronic myeloproliferative disorders (V617F detection and exon 12 sequencing of JAK2 gene)
CHU de Bordeaux-GH Sud - Hôpital Haut-Lévêque
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

KIT (D816V): Molecular diagnosis of Chronic Myeloid Leukaemia (BCR/ABL1: by PCR, RT-PCR and FISH)
Cambridge University Hospitals NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Technical procedure(s) : PCR based techniques, FISH

SPAIN

Cataluña
TARRAGONA

Molecular diagnosis of essential thrombocythemia (JAK2 gene / mutation V617F; CALR gene / mutations in exon 9)
Hospital Universitari de Tarragona Joan XXIII
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

ITALY

LOMBARDIA
VARESE

Molecular diagnosis of essential thrombocythemia (CALR gene)
A.O.U. Ospedale di Circolo e Fondazione Macchi - Università dell'Insubria
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)

ITALY

LOMBARDIA
VARESE

Molecular diagnosis of myeloproliferative neoplasm (JAK2 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)

ITALY

LOMBARDIA
PAVIA

Cytogenetic, molecular and molecular cytogenetic diagnosis of essential thrombocythemia
Fondazione IRCCS Policlinico San Matteo
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics

CZECH REPUBLIC

South Moravia
BRNO

Molecular diagnosis of myeloproliferative neoplasms (JAK2 gene)
University hospital Brno
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Greater Manchester
MANCHESTER

Molecular diagnosis of Polycythaemia Vera, Essential Thrombocythaemia and Idiopathic Myelofibrosis by JAK2 analysis
Central Manchester University Hospitals - Manchester Royal Infirmary
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

ITALY

PUGLIA
SAN GIOVANNI ROTONDO

Molecular diagnosis of essential thrombocythemia (JAK2 gene)
IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

ITALY

CALABRIA
REGGIO CALABRIA

Molecular diagnosis of essential thrombocythemia (JAK2 gene)
Azienda Ospedaliera BMM
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
CRÉTEIL

Molecular diagnosis of myeloproliferative syndromes (JAK2 gene : V617F mutation ; TET2)
CHU Henri Mondor
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

LEBANON

Beyrouth
BEIRUT

Molecular diagnosis of myeloproliferative syndromes (V617F mutation of JAK2 gene)
Université Saint-Joseph
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

ROMANIA

CLUJ
CLUJ-NAPOCA

Molecular diagnosis of chronic myeloproliferative diseases (V617F mutation of JAK2 gene)
Spitalul Judetean Clinc de Urgenta Cluj
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

SLOVENIA

SLOVENIA
LJUBLJANA

Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene: V617F mutation)
University Medical Center Ljubljana
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

ALSACE
COLMAR

Molecular diagnosis of myeloproliferative syndromes (JAK2 gene : V617F mutation)
Hôpital Pasteur - Hôpitaux civils de Colmar
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

SERBIA

Serbia
BELGRADE

Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene: mutation V617F)
Institute of Molecular Genetics and Genetic Engineering
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

PROVENCE-ALPES-COTE D'AZUR
NICE

Molecular diagnosis of myeloproliferative syndromes (JAK2 gene: V617F mutation)
CHU de Nice - Hôpital Pasteur
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

LANGUEDOC-ROUSSILLON
NÎMES

Molecular diagnosis of chronic myeloproliferative disorders (JAK2 gene: V617F)
CHU de Nîmes - Hôpital Caremeau
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

CHAMPAGNE-ARDENNE
TROYES

Molecular diagnosis of chronic myeloproliferative disorders (JAK2 and MPL genes)
CH de Troyes - Hôpital des Hauts-Clos
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

ITALY

LOMBARDIA
BRESCIA

Molecular diagnosis of myeloproliferative diseases (JAK2 gene)
Biodiversity
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

LITHUANIA

DZUKIJA
VILNIUS

Molecular diagnosis of myeloproliferative disorders (JAK2 gene:mutation V617F)
Vilnius University Hospital Santariskiu Klinikos
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

Olomouc
OLOMOUC

Molecular diagnosis of myeloproliferative disorders (JAK2 gene)
University hospital Olomouc
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

PICARDIE
AMIENS

Molecular diagnosis of myeloproliferative disorders (JAK2 gene)
CHU Amiens-Picardie - Site Sud
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

South Bohemia
CESKE BUDEJOVICE

Molecular diagnosis of myeloproliferative disorders (JAK2 gene)
Hospital Ceské Budejovice
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of essential thrombocythemia (CALR, MPL, JAK2 genes/V617F, K539L and V607N mutations)
Laboratorio de Genética Clínica, S.L.
Purpose(s) : Antenatal diagnosis, Pre-symptomatic diagnosis, Somatic genetics
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

SPAIN

La Rioja
LOGROÑO

Molecular diagnosis of essential thrombocythemia (JAK2 gene)
Hospital San Pedro
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

SPAIN

Madrid
MAJADAHONDA

Molecular diagnosis of myeloproliferative disorders related to JAK2
Genyca Innova
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

POLAND

Warszawa
WARSAW

Molecular diagnosis of myeloproliferative syndromes (V617F mutation in JAK2 gene)
IHIT Instytut Hematologii I Transfuzjologii
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

SPAIN

Galicia
A CORUÑA

Molecular cytogenetics and molecular diagnosis of chronic myeloproliferative disorders (t(9;22) [BCR/ABL] - FISH/PCR/QPCR, JAK2 gene - V617F mutation, exon12 (PCR))
Complejo Hospitalario Universitario A Coruña
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Technical procedure(s) : PCR based techniques, FISH

FRANCE

BRETAGNE
RENNES

Molecular diagnosis of myeloproliferative neoplasm (JAK2 gene by PCR, QPCR)
CHU de Rennes - Hôpital Pontchaillou
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technical procedure(s) : PCR based techniques

MOROCCO

Rabat
RABAT

Molecular diagnosis of myeloproliferative syndromes (V617F mutation in JAK2 gene)
Institut National d'Hygiène
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

MOROCCO

Rabat
RABAT

Molecular diagnosis of myelofibrosis with myeloid metaplasia, essential thrombocythemia (Exon 9 of CALR gene)
Institut National d'Hygiène
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

BASILICATA
MATERA

Postnatal molecular diagnosis of myeloproliferative syndromes (V617F mutation in JAK2 gene)
Presidio Ospedaliero "Madonna delle Grazie" - Azienda Sanitaria di Matera (ASM)
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technical procedure(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of hemorrhagic disorders due to a constitutional platelet anomaly (Panel)
CHU Paris - Hôpital Robert Debré
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)

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of myeloproliferative neoplasm (Panel)
CHU Paris-GH St-Louis Lariboisière F.Widal - Hôpital Saint-Louis
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)

AUSTRIA

WIEN
WIEN

Molecular cytogenetic diagnosis of myeloproliferative neoplasms (t(9;22)(q34;q11); BCR-ABL amplification, +8, +9, +21, -5/5q-, -7/7q-, 20q-, 13q-, 12p-, i(17q), CHIC2-deletion (FIP1L1/PDGFRa rearrangement), rearrangements of PDGFRa, -b, FGFR1; further analyses upon request)
Labordiagnostik GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technical procedure(s) : M-FISH/SKY, FISH