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FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of Ewing sarcoma
CLCC Institut Curie
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

SPAIN

Madrid
MAJADAHONDA

Accreditation
Diagnosis of Ewing sarcoma (fusion genes EWSR1/FLI1, EWSR1/ERG)
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

GREECE

ATTIKI
ATHENS

Accreditation
Molecular and molecular cytogenetic diagnosis of Ewing sarcoma (EWS-FLI, EWS-ERG and EWS-ETV1 genes)
BioAnalytica-GenoType SA
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics

UNITED KINGDOM

Lanarkshire
GLASGOW

Accreditation
Molecular and molecular cytogenetic diagnosis of Ewing sarcoma (EWSR1, FLI1 and ERG: by FISH and RT-PCR)
Queen Elizabeth University Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Technique(s) : PCR based techniques, FISH

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Ewing Sarcoma (RT-PCR analysis EWSR1/FLI1; EWSR1/ERG)
Mount Sinai Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

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 Paris-Trousseau thrombocytopenia (FLI1 gene)
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

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

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)

FRANCE

GRAND-EST
VANDOEUVRE-LÈS-NANCY

Accreditation
Diagnosis of intellectual disability and/or epilepsy (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) : Whole Exome Sequencing (WES)

BELGIUM

OOST-VLAANDEREN
GENT

Accreditation
Diagnosis of congenital structural heart defects (gene panel)
Centrum Medische Genetica Gent - Universitair Ziekenhuis Gent
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
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)

AUSTRALIA

Victoria
MELBOURNE

Accreditation
Molecular diagnosis of Ewing sarcoma (analysis of fusion transcripts: EWSR1-FLI1 ; EWSR1-ERG)
Monash Health
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

LITHUANIA

DZUKIJA
VILNIUS

Molecular diagnosis of Ewing sarcoma (EWSR1-FLI1, EWSR1-ERG, EWSR1-ETV1, EWSR1-ETV4 fusion genes)
Vilnius University Hospital Santariskiu Klinikos
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

CANADA

Québec
QUÉBEC

Molecular diagnosis of Ewing Sarcoma (t(11;22) EWSR1-FLI1 + t(21;22) EWSR1-ERG)
CHUQ - Centre Hospitalier Universitaire de Québec - Hôtel-Dieu de Québec
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics