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Caption : Accreditation =Accreditation
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GERMANY

Niedersachsen
HANNOVER

Accreditation
Diagnosis of acute lymphoblastic leukemia (fusion or rearrangements: AF4-MLL, BCR-ABL, TEL-RUNX1 (TEL-AML1), MLL, E2A-PBX1, MYC-IGH, TCRA/D, IGH, MYC)
Medizinische Hochschule Hannover
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : PCR based techniques, FISH

FRANCE

HAUTS-DE-FRANCE
LILLE

Accreditation
Diagnosis of fibrosarcoma : search for ETV6/NTRK3 fusion gene
CHU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

UNITED KINGDOM

West Midlands
BIRMINGHAM

Accreditation
Molecular diagnosis of Acute Lymphoblastic Leukemia (by detection of fusion transcripts: BCR-ABL and ETV6/RUNX1, RQ-PCR: BCR-ABL and TCRB and TCRG PCR for B and T cell clonality studies)
Birmingham Women's NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

GREECE

ATTIKI
ATHENS

Accreditation
Molecular and molecular cytogenetic diagnosis of acute lymphoblastic leukemia (detection by FISH and qRT-PCR of TEL-AML1, BCR-ABL and MLL genes)
BioAnalytica-GenoType SA
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Technique(s) : PCR based techniques, FISH

FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation
Diagnosis of hereditary thrombocytopenia with normal PMV (RUNX1, ETV6 genes)
CHU de Marseille - Hôpital de la Timone
Purpose(s) : Post-natal diagnosis, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

SPAIN

Madrid
MAJADAHONDA

Accreditation
Diagnosis of fibrosarcoma (ETV6/NTRK3 fusion gene)
Instituto de Salud Carlos III. Campus de Majadahonda
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

GERMANY

Bayern
MARTINSRIED/PLANEGG

Accreditation
Diagnosis of acute lymphoblastic leukemia (BCR-ABL1, MLL, MLL-AF4, MLL-ENL, MLL-AF9, ETV6-RUNX1, E2A-PBX)
MVZ Martinsried GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Diagnosis of acute myeloid leukemia
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics, Immunology
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : Sanger sequencing, PCR based techniques, FISH, Karyotyping

GERMANY

Bayern
MARTINSRIED/PLANEGG

Accreditation
Diagnosis of acute lymphoblastic leukemia
MVZ Martinsried GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region, Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : NGS sequencing (except WES), PCR based techniques, FISH, Karyotyping

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of autosomal thrombocytopenia with normal platelets (ANKRD26 and ETV6 genes)
AP-HP.Sorbonne Université - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

Accreditation
Molecular and molecular cytogenetic diagnosis of Acute Lymphoblastic Leukemia (TAL1, TCF3/PBX1, MLL/AFF1 and TEL/AML1: by PCR, RT-PCR and FISH)
Cambridge University Hospitals NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Technique(s) : PCR based techniques, FISH

GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Diagnosis of chronic myelomonocytic leukemia
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics, Immunology
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region, Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : Sanger sequencing, PCR based techniques, FISH, Karyotyping

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of predisposition to hemopathies (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
Technique(s) : NGS sequencing (except WES)

FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation
Diagnosis of hemorrhagic disorders due to a constitutional platelet anomaly (Panel)
CHU de Marseille - Hôpital de la Timone
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of myelodysplastic syndrome and myelodysplastic acute leukemia (Panel)
GHU AP-HP Nord. Université de Paris - Hôpital Saint-Louis
Purpose(s) : 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, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Sanger sequencing, PCR based techniques

GERMANY

Bayern
MÜNCHEN

Accreditation
Diagnosis of acute lymphoblastic leukemia (BCR, CDKN2A, ETV6, FLT3, PDGFRA, PICALM, RUNX1 genes)
Pränatal-Medizin München MVZ GmbH
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : Sanger sequencing, MLPA based techniques

GERMANY

Bayern
MÜNCHEN

Accreditation
Diagnosis of chronic myelomonocytic leukemia (ETV6, PDGFRB genes)
Pränatal-Medizin München MVZ GmbH
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of hemorrhagic disorders due to a constitutional platelet anomaly (Panel)
AP-HP.Sorbonne Université - Hôpital d'Enfants Armand-Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of thrombocytopenia (Panel)
CHU Paris - Hôpital Robert Debré
Purpose(s) : Pre-implantation diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES), Sanger sequencing

GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Diagnosis of acute lymphatic leukaemia
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics, Immunology
Objective(s) : Targeted mutation analysis, Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : PCR based techniques, FISH, Karyotyping

NETHERLANDS

Utrecht
UTRECHT

Accreditation
Molecular diagnosis of Primary Haemostasis (gene panel; TRO02v17.1)
UMC Utrecht - Universitair Medisch Centrum Utrecht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

GERMANY

Baden-Württemberg
TÜBINGEN

Accreditation
Molecular analysis of somatic mutation in tumour tissue for therapeutic decisions (Somatic Tumor Panel, 710 genes)
CeGaT GmbH
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

GERMANY

Mecklenburg-Vorpommern
GREIFSWALD

Accreditation
Diagnosis of thrombocytopenias and thrombocytopathies (NGS screening panel, 26 genes)
Institut für Humangenetik der Universitätsmedizin Greifswald
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

GERMANY

Baden-Württemberg
TÜBINGEN

Accreditation
Diagnosis of hematopoietic defects (NGS screening panel: 183 genes)
CeGaT GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES)

BELGIUM

LIEGE
LIEGE

Accreditation
Diagnosis of myeloid neoplasms with germline predisposition (gene panel)
CHU de Liège - UniLab Lg
Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : NGS sequencing (except WES)

BELGIUM

VLAAMS BRABANT
LEUVEN

Accreditation
Diagnosis of coagulation disorders (gene panel)
UZ Leuven - Campus Gasthuisberg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Accreditation
Diagnosis of inherited hematologic cancer-predisposing syndrome (Panel)
CLCC Institut Paoli Calmettes
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, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

BELGIUM

LIEGE
LIEGE

Accreditation
Diagnosis of congenital hematological disorders (gene panel)
CHU de Liège - UniLab Lg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Whole Exome Sequencing (WES)

BELGIUM

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Accreditation
Molecular diagnosis of Acute Lymphoblastic Leukaemia (TEL-AML1,E2A-PBX1,BCR-ABL1, WT1)
Erasme Hospital - ULB
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing

CANADA

Ontario
HAMILTON

Accreditation
Molecular Diagnosis of Acute Lymphoid Leukemia (RNA analysis)
McMaster University Medical Centre
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

SPAIN

Comunidad Valenciana
VALENCIA

Diagnosis of acute lymphoblastic leukemia (MLL gene and ETV6/ RUNX1 fusion gene)
Hospital Universitario y Politécnico La Fe
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

ITALY

CAMPANIA
NAPOLI

Diagnosis of acute lymphoblastic leukemia (BCR/ABL1, E2A/PBX1, MLL/AF4, MLL/ENL, TEL/AML1 rearrangement)
Biotecnologie Avanzate Srl
Purpose(s) : 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
Technique(s) : Sanger sequencing

SPAIN

Comunidad Valenciana
PATERNA

Diagnosis of precursor B-cell acute lymphoblastic leukemia (ABL1, AFF1, BCR, ETV6, KMT2A, PBX1, RUNX1, TCF3 genes)
IMEGEN - Delegación Valencia
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : NGS sequencing (except WES)

FRANCE

BRETAGNE
RENNES

Diagnosis of precursor B-cell acute lymphoblastic leukemia (BCR-ABL1, RUNX1- ATV6, KMT2A-AFF1, IKZF1 genes by RT-PCR, RQ-PCR, PCR, QPCR, MLPA)
CHU de Rennes - Hôpital Pontchaillou
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques, MLPA based techniques

AUSTRIA

WIEN
WIEN

Diagnosis of myelodysplastic/myeloproliferative diseases (analysis block: ASXL1, CBL, DNMT3A, ETV6, EZH2, IDH1, IDH2, JAK2, KRAS, NRAS, RUNX1, SF3B1, SRSF2, TET2, TP53, U2AF1, ZRSR2 gene)
Hanusch Krankenhaus
Purpose(s) : Somatic genetics, Risk assessment
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

FRANCE

NOUVELLE AQUITAINE
PESSAC

Diagnosis of acute lymphoblastic leukemia (detection of MLL-AFF1, TCF3-PBX1, ETV6-RUNX1 and STIL-TAL1 fusion genes)
CHU de Bordeaux-GH Sud - Hôpital Haut-Lévêque
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

SLOVENIA

SLOVENIA
LJUBLJANA

Molecular and cytogenetic diagnosis of acute lymphoblastic leukemia (TEL/AML1, BCR/ABL, TCF3/PBX1, ETV6/RUNX1gene fusions; FISH and conventional karyotype)
University Medical Center Ljubljana
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Detection of chromosome alterations large in size
Technique(s) : Sanger sequencing, Karyotyping

SERBIA

Serbia
BELGRADE

Molecular diagnosis of acute lymphoblastic leukemia (RT-PCR analysis of BCR-ABL1, MLL-AFF1, ATV6-AML1 and PBX1-TCF3 fusion genes)
Mother and Child Health Institute of Serbia "Dr Vukan Cupic"
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

SERBIA

Serbia
BELGRADE

'Molecular diagnosis of acute lymphoblastic leukemia (detection of BCR-ABL, MLL-AFF1, TEL-AML1 and E2A-PBX1 fusion transcripts; rearrangements of IGH and CD3G loci)'
Institute of Molecular Genetics and Genetic Engineering
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

LITHUANIA

DZUKIJA
VILNIUS

Molecular diagnosis of acute lymphoblastic leukemia (detection of BCR-ABL, MLL-AFF1, TEL-AML1 and E2A-PBX1 fusion transcripts)
Vilnius University Hospital Santariskiu Klinikos
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

CANADA

Québec
QUÉBEC

Molecular diagnosis of chronic myelomonocytic leukemia - t(5;12) (ETV6/PDGFRb genes)
CHUQ - Centre Hospitalier Universitaire de Québec - Hôtel-Dieu de Québec
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

HAUTS-DE-FRANCE
LILLE

Diagnosis of tumors of hematopoietic tissues (Panel)
CHU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

SPAIN

Cataluña
BADALONA

Diagnosis of myeloid hemopathy (panel)
ICO Badalona - Hospital Germans Trias i Pujol
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

SPAIN

Madrid
MADRID

Diagnosis of myeloid hemopathy (panel)
Hospital General Universitario Gregorio Marañón
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)