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FRANCE

OCCITANIE
MONTPELLIER

Accreditation
Diagnosis of malignant hemopathies
CHU de Montpellier - Hôpital Saint-Eloi
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics

GERMANY

Thüringen
JENA

Accreditation
Diagnosis of myeloproliferative disorders (PDGFRA and PDGFRB gene aberrations)
Institut für Humangenetik am Universitätsklinikum Jena
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : FISH, Karyotyping

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

UNITED KINGDOM

Nottinghamshire
NOTTINGHAM

Accreditation
Molecular cytogenetic diagnosis of Acute Myeloid Leukaemia (by karyotyping and FISH)
Nottingham University Hospitals NHS Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

UNITED KINGDOM

Oxfordshire
OXFORD

Accreditation
Cytogenetic diagnosis of Acute Myeloid Leukaemia
Churchill Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

IRELAND

County Dublin
DUBLIN

Accreditation
Molecular cytogenetic diagnosis of Myelodysplastic syndrome (by conventional karyotype and FISH)
Children's Health Ireland @ Crumlin
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : FISH, Karyotyping

GERMANY

Berlin
BERLIN

Accreditation
Diagnosis of myelodysplastic/myeloproliferative diseases
Labor Berlin - Charité Vivantes GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

FRANCE

GRAND-EST
METZ

Accreditation
FISH diagnosis of hemopathies
CHR de Metz-Thionville
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

UNITED KINGDOM

Grampian
ABERDEEN

Accreditation
Molecular diagnosis of Myeloproliferative disorders (JAK2 gene)
Aberdeen Royal Infirmary, Polwarth Building
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Antrim and Newtownabbey
BELFAST

Accreditation
Molecular cytogenetic diagnosis of Myelodysplastic syndrome/myeloproliferative disease (by FISH analysis)
Belfast City Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

UNITED KINGDOM

South Yorkshire
SHEFFIELD

Accreditation
Molecular cytogenetic diagnosis of Myelodysplastic syndromes (by karyotyping and FISH analysis)
Sheffield Children's NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

West Midlands
BIRMINGHAM

Accreditation
Cytogenetic diagnosis of Myelodysplastic syndrome (by conventional karyotype)
Birmingham Women's NHS Foundation Trust
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

Wiltshire
SALISBURY

Accreditation
Cytogenetic diagnosis of Myelodysplastic syndrome (by conventional karyotype)
Salisbury District Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

Nottinghamshire
NOTTINGHAM

Accreditation
Molecular cytogenetic diagnosis of Myelodysplastic syndrome (by karyotyping and FISH)
Nottingham University Hospitals NHS Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

UNITED KINGDOM

Avon
BRISTOL

Accreditation
Molecular cytogenetic diagnosis of Myelodysplastic syndrome (by FISH)
Southmead Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : FISH

UNITED KINGDOM

South Glamorgan
CARDIFF

Accreditation
Molecular cytogenetic diagnosis of Myelodysplastic syndrome (by conventional karyotyping and FISH)
University Hospital of Wales
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

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

SWITZERLAND

Suisse Romande
GENÈVE

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

CANADA

Ontario
MISSISSAUGA

Accreditation
Molecular Cytogenetic Solid Tumor Analysis (Paraffin Embedded Tissue ALK, MYC, ERBB2)
Trillium Health Partners- Credit Valley Site
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

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

GRAND-EST
VANDOEUVRE-LÈS-NANCY

Accreditation
Diagnosis of malignant hemopathies
CHU de Nancy - Hôpitaux de Brabois
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

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)

FRANCE

ILE-DE-FRANCE
SAINT-OUEN-L'AUMÔNE

Accreditation
Diagnosis of hematologic neoplams
Laboratoire Cerba
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : NGS sequencing (except WES), FISH, Karyotyping

FRANCE

NORMANDIE
ROUEN

Accreditation
Diagnosis of rare genetic tumor (Phenotyping in oncogenetics) (Whole exome)
CHU de Rouen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Whole Exome Sequencing (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)

FRANCE

HAUTS-DE-FRANCE
AMIENS

Accreditation
Diagnosis of family predisposition to myeloid diseases (Panel)
CHU Amiens-Picardie - Site Sud
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

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)

UNITED KINGDOM

Surrey
SURREY

Accreditation
Cytogenetic diagnosis of Myelodysplastic syndrome (by conventional karyotype)
Institute of Cancer Research ICR
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

Lanarkshire
GLASGOW

Accreditation
Cytogenetic diagnosis of Acute Myeloid Leukaemia by conventional cytogenetics (AML/ETO, PML/RARA, CBFB & MLL)
Queen Elizabeth University Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

Lanarkshire
GLASGOW

Accreditation
Cytogenetic diagnosis of Myelodysplastic syndrome (by conventional karyotype)
Queen Elizabeth University Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

GERMANY

Schleswig-Holstein
KIEL

Accreditation
Diagnosis of chronic myelomonocytic leukemia (BCR (22q11)/ABL (9q34), FGFR1 (8p12), FIP1L1/CHIC2/PDGFRA (4q12), PDGFRB (5q33))
Praxis Dr. Lana Harder
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by CXCR4 Exon 2, DNMT3A Exon 23, FLT3 Exon 20 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Other
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)

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of myelodysplastic/myeloproliferative disease and B-cell chronic lymphocytic leukemia (BCR/ABL mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Hematology, Other

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for CALR Exon 9 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of hemopathies (P190 mutation / transmitted analysis)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for NRAS Exons 2 and 3 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for IDH2 Exon 4 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : NGS sequencing (except WES)

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Research for paroxysmal nocturnal hemoglobinuria (HNP clone)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Hematology, Other

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of hemopathies (by looking for TXL1 transcript)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of hemopathies (by looking for TXL3 transcript)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of hemopathies (by looking for SIL-TAL transcript)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of hemopathies (by looking for TEL-AML1 transcript)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of hemopathies (by looking for PML-RARA transcript)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Search for E2A-PBX transcript
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of hemopathies (by looking for NPM1 transcript)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of hemopathies (by looking for DEK-CAN transcript)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of hemopathies (by looking for BCR ABL1 or CALM-AF10 transcript)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of hemopathies (by looking for AML1-ETO or CBFB-MYH11 transcript)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for STAT3 Exons 20 and 21 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for TP53 Exons 4 to 10 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for GATA2 Exons 2,3,4,5,6 and intron 4 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for KRAS Exons 2 and 3 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of LAM, MDS, LMMC and medluar aplasie
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by RUNX1 exons 3 to 8, SETBP1 exon 4, PTEN exons 1,2,5,6,7,8, or SF3B1 exons 14 to 16 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by SRSF2 Exon 1, KRAS exons 2 and 3, NOTCH1 exons 26,27,28 and 34 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for BTK exon 15, JAK2-Exon 12 or PLCG2 exons 19,20 and 24 mutation,)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : NGS sequencing (except WES)

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for LALT IKAROS (IKZF1) LALB or PTEN deletion)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis
Technique(s) : MLPA based techniques

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for JAK2 V617F mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : NGS sequencing (except WES)

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for MYD88 L265P or KIT Exons 8,9,11,13,17 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for BCR/ABL mutation/ transmitted exam)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of lymphoid and myeloid hemopathy (by looking for NPM1 Exon 12 mutation)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : NGS sequencing (except WES)

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of tumor of hematopoietic and lymphoid tissues (mutational status genes immunoglobulin)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics, Hematology
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

FRANCE

OCCITANIE
TOULOUSE

Accreditation
Diagnosis of myelomonocytic leukemia (Culture of progenitors leukemics)
IUCT Oncopole - CHU Toulouse
Purpose(s) : Somatic genetics
Specialty(ies) : Hematology

UNITED KINGDOM

Greater London
LONDON

Molecular cytogenetic diagnosis of Acute Myeloid Leukaemia (by conventional karyotype and FISH analysis)
Hammersmith Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

UNITED KINGDOM

Greater London
LONDON

Molecular cytogenetic diagnosis of Myeloproliferative disorder (by conventional karyotype and FISH analysis)
Hammersmith Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

TURKEY

TURKEY
ISTANBUL

Molecular diagnosis of chronic myelomonocytic leukaemia (PDGFRB gene)
Genetiks - Genetic diagnosis and research center
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

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

ITALY

UMBRIA
PERUGIA

Cytogenetic and molecular cytogenetic diagnosis of myelodysplastic/myeloproliferative diseases
Università degli Studi di Perugia - Ospedale S. Maria della Misericordia
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics

UNITED KINGDOM

Tayside
DUNDEE

Cytogenetic diagnosis of Acute Myeloid Leukaemia
Ninewells Hospital and Medical School
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

Tyne & Wear
NEWCASTLE UPON TYNE

Cytogenetic diagnosis of Acute Myeloid Leukaemia
Newcastle upon Tyne Hospitals NHS Trust
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

Tayside
DUNDEE

Cytogenetic diagnosis of Myelodysplastic syndrome
Ninewells Hospital and Medical School
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

Greater London
LONDON

Molecular cytogenetic diagnosis of Myelodysplastic syndrome (MECOM: by FISH analysis)
University College London Hospitals, NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

GERMANY

Nordrhein-Westfalen
KÖLN

Diagnosis of myelodysplastic syndromes (EGR1 (5q31), D5S23/D5S721 (5p15.2), CEP7 (7p11.1-q11.1), D7S486 (7q31), CEP8 (8p11.1-q11.1), TP53 (17p13.1), D20S108 (20q12))
Zotz|Klimas Standort Köln
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of microdeletions/microduplications
Technique(s) : FISH

GERMANY

Nordrhein-Westfalen
KÖLN

Diagnosis of chronic myelomonocytic leukemia (CEP7 (7p11.1-q11.1), D7S486 (7q31), CEP8 (8p11.1-q11.1), D20S108 (20q12))
Zotz|Klimas Standort Köln
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

FRANCE

GRAND-EST
STRASBOURG

Diagnosis of myeloid hemopathies (classical caryotype and FISH)
CHU de Strasbourg - Hôpital de Hautepierre
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

FRANCE

OCCITANIE
TOULOUSE

Diagnosis of myeloid hemopathies
IUCT Oncopole - CLCC Institut Claudius Regaud
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

SPAIN

Cataluña
BARCELONA

Diagnosis of myelodysplastic/myeloproliferative disease
Hospital de la Santa Creu i Sant Pau
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

SPAIN

Cataluña
BADALONA

Diagnosis of myelodysplastic/myeloproliferative disease
ICO Badalona - Hospital Germans Trias i Pujol
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

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)

AUSTRIA

WIEN
WIEN

Diagnosis of chronic myelomonocytic leukemia (MDS panel plus 8p12 (FGFR1 break apart probe), 3q21 (EVI1 break apart probe), 3q21-26 (RPN1/MECOM))
Hanusch Krankenhaus
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

UNITED KINGDOM

Dorset
BOURNEMOUTH

Molecular cytogenetic diagnosis of Myelodysplastic syndrome (by FISH analysis)
Royal Bournemouth Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

GERMANY

Rheinland-Pfalz
KAISERSLAUTERN

Diagnosis of chronic myelomonocytic leukemia (del7q31; +8; MLL; del20q12)
Med-Biolog-Labor
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

PORTUGAL

NORTE
PORTO

Molecular cytogenetic diagnosis of malignant haemopathies
Instituto Português de Oncologia do Porto Francisco Gentil, EPE
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

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

Cataluña
BADALONA

Diagnosis of chronic myelomonocytic leukemia (ASXL1 gene / exon 12; SRSF2 gene / exon 1)
ICO Badalona - Hospital Germans Trias i Pujol
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

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)

SPAIN

Asturias
OVIEDO

Diagnosis of chronic myelomonocytic leukemia
Hospital Universitario Central de Asturias
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping