x

Search for a diagnostic test

* (*) mandatory field

37 Result(s)

Filter by

Speciality(ies)/objective(s)

Technique(s)

Purpose(s)

Quality management

Country(ies)

Reset
Sort by

Caption : Accreditation =Accreditation
;

GERMANY

Niedersachsen
HANNOVER

Accreditation
Diagnosis of acute myeloblastic leukemia (fusion genes and rearrangements: RUNX1-RUNX1T1 (AML1-ETO), CBFB-MYH11, PML-RARA, MLLT3-MLL (AF9-MLL), DEK-NUP214 (DEK-CAN), RPN1-EVI1, RBM15-MKL1, MLL, RUNX1-EVI1; aberrations of chromosom 17 (17p13 / TP53), 5/5q, 7/7q; mutation analysis of FLT-TKD, WT1, C- KIT, N- RAS, GATA1, GATA2, RUNX1 (AML1), CEBPA)
Medizinische Hochschule Hannover
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region, Detection of microdeletions/microduplications
Technique(s) : Sanger sequencing, PCR based techniques, FISH

UNITED KINGDOM

Devon
PLYMOUTH

Accreditation
Molecular diagnosis of Acute Myeloid Leukaemia - t(8;21), inv(16) and FLT3 internal tandem duplications
Plymouth Derriford Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : PCR based techniques

UNITED KINGDOM

West Midlands
BIRMINGHAM

UNITED KINGDOM

Avon
BRISTOL

Accreditation
Molecular haemato-oncology diagnosis of Acute Myeloid Leukaemia (FLT3 gene: itd & NPM1 gene: exon 12 mutation)
Southmead Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

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

UNITED KINGDOM

Wiltshire
SALISBURY

Accreditation
Molecular diagnosis of Acute leukaemia with ambigous lineage (FLT 3 gene: common duplication)
Salisbury District Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Deletion / Duplication analysis

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

Accreditation
Molecular and molecular cytogenetic diagnosis of Acute Myeloid Leukaemia (FLT3, NPM1, RUNX1-RUNX1T1, CBFB-MYH11, PML/RARA and MLL: 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

Bayern
MÜNCHEN

Accreditation
Diagnosis of acute lymphoblastic leukemia (BCR, CDKN2A, ETV6, FLT3, PDGFRA, PICALM, RUNX1 genes)
Pränatalmedizin München
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 acute myeloid leukemia with t(8;21)(q22;q22) (CEBPA, FLT3, KIT, RUNX1 genes)
Pränatalmedizin München
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

GERMANY

Bayern
MÜNCHEN

Accreditation
Diagnosis of acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) (FLT3, KIT genes)
Pränatalmedizin München
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

GERMANY

Bayern
MÜNCHEN

Accreditation
Diagnosis of acute myeloid leukemia with/without matuation or minimal differentiation (FLT3, KIT, NPM1 genes)
Pränatalmedizin München
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 myeloid hemopathy (Panel)
CHU de Nancy - Hôpitaux de Brabois
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

SWEDEN

Landstinget i Östergötland
LINKÖPING

Accreditation
Molecular diagnosis of acute myeloid leukemia (FLT3 and CEBPA genes)
Universitetssjukhuset i Linköping
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics

GERMANY

Bayern
MARTINSRIED

Accreditation
Diagnosis of acute myeloid leukemia (FLT3 gene: ITD and D835, JAK2 gene: V617F/G1849T, NPM1 gene: exon 12, t(8; 21), t(15; 17), inv(16))
LabPMM GmbH
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Acute Myeloid Leukemia (AML/ETO, BCR/ABL, CBFB/MYH11, FLT3/NPM1, PML/RARA, KIT PCR analysis)
Toronto General Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

CANADA

Ontario
HAMILTON

Accreditation
Molecular Diagnosis of Acute Myeloid Leukemia (AML/ETO, BCR/ABL, CBFB/MYH11, FLT3/NPM1, PML/RARA, RNA analysis)
McMaster University Medical Centre
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of myelodysplastic syndrome and myelodysplastic acute leukemia (Panel)
CHU Paris-GH St-Louis Lariboisière F.Widal - 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

SPAIN

Comunidad Valenciana
VALENCIA

Diagnosis of acute myeloid leukemia (FLT3, NPM1 genes and RUNX1/ RUNX1T1, CBFb/MYH11 fusion genes)
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) : NGS sequencing (except WES), PCR based techniques

TURKEY

TURKEY
ISTANBUL

Molecular diagnosis of acute lymphoblastic leukaemia (FLT3 gene)
Genetiks - Genetic diagnosis and research center
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

TURKEY

TURKEY
ISTANBUL

Molecular diagnosis of acute myeloid leukaemia (FLT3 gene)
Genetiks - Genetic diagnosis and research center
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

ITALY

LOMBARDIA
VARESE

Molecular diagnosis of acute leukemia of ambiguous lineage (FLT3 gene)
A.O.U. Ospedale di Circolo e Fondazione Macchi - Università dell'Insubria
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : NGS sequencing (except WES)

UNITED KINGDOM

Surrey
SURREY

Molecular diagnosis of Acute Myeloid Leukaemia (PML/RARA, RUNX1T1-RUNX1, inv(16), BCR/ABL and FLT3-ITD/D835 mutations)
Institute of Cancer Research ICR
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Diagnosis of acute myeloid leukemia (FLT3 gene)
Centogene AG
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

AUSTRIA

WIEN
WIEN

Diagnosis of acute myeloid leukemia (t(8;21)(q22;q22); FLT3 gene)
Hanusch Krankenhaus
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Sequence analysis: entire coding region, Detection of chromosome alterations large in size
Technique(s) : NGS sequencing (except WES), Sanger sequencing, FISH

AUSTRIA

WIEN
WIEN

Diagnosis of acute lymphoblastic leukemia (t(9;22)(q34;q11) (BCR/ABL); ABL-tyrosine kinase domain; FLT3 gene analysis)
Hanusch Krankenhaus
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
Technique(s) : NGS sequencing (except WES), Sanger sequencing, FISH

CYPRUS

Cyprus
NICOSIA

Molecular diagnosis of acute myeloid leukemia : search for FLT3 gene mutations and for BCR/ABL1and AML1/ETO fusion genes
Karaiskakio foundation
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

NOUVELLE AQUITAINE
PESSAC

'Diagnosis of acute lymphoblastic leukemia (detection of CBFB-MYH11, PML-RARA, RUNX1-RUNX1T1 fusion genes; FLT3 and NPM1 gene sequencing)'
CHU de Bordeaux-GH Sud - Hôpital Haut-Lévêque
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
Technique(s) : Sanger sequencing, PCR based techniques

SLOVENIA

SLOVENIA
LJUBLJANA

'Molecular and cytogenetic diagnosis of acute myeloid leukemia (sequencing of gene fusions in t(15;17), t(8;21), inv(16); FISH)'
University Medical Center Ljubljana
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

SERBIA

Serbia
BELGRADE

'Molecular diagnosis for prognostic groups in acute myeloid leukemia (NPM1 gene: mutations in exon 12; FLT3: mutation detection comprising D835)'
Institute of Molecular Genetics and Genetic Engineering
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

LITHUANIA

DZUKIJA
VILNIUS

Molecular diagnosis of acute myeloid leukemia (detection of PML-RARA, AML1-ETO, DEK-CAN, CBFB-MYH11 fusion transcripts; NPM1 and FLT3 mutations
Vilnius University Hospital Santariskiu Klinikos
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

CANADA

Québec
QUÉBEC

Molecular diagnosis of acute myeloid leukemia (detection of PML-RARa, AML1-ETO, CBFB-MYH11 fusion transcripts; NPM1, CEPBa and FLT3 mutations)
CHUQ - Centre Hospitalier Universitaire de Québec - Hôtel-Dieu de Québec
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GERMANY

Berlin
BERLIN

Diagnosis of cancer (NGS screening panel, 402 genes)
ATG GenMed 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)

SPAIN

Madrid
MADRID

Molecular diagnosis of acute biphenotypic leukemia (PCR FLT3)
Hospital General Universitario Gregorio Marañón
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of acute myeloid leukemia (NPM1, FLT3, KIT genes)
LabGenetics - Laboratorio de Genética Clínica, S.L.
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

Cataluña
BADALONA

Diagnosis of acute myeloid leukemia (FLT3 gene / mutation and internal tandem duplication (FLT3-ITD) and FLT3-TKD mutation)
ICO Badalona - Hospital Germans Trias i Pujol
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Deletion / Duplication analysis
Technique(s) : Sanger sequencing, PCR based techniques

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)