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FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Molecular diagnosis of rhabdoid tumors (SMARCB1 and SMARCA4 genes)
CLCC Institut Curie
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

NETHERLANDS

Zuid-Holland
ROTTERDAM

Accreditation
Molecular diagnosis of Rhabdoid Tumors (SMARCB1 gene)
Erasmus MC, Faculteitsgebouw
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : Sanger sequencing, MLPA based techniques

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of predisposition to rhabdoid tumors (Panel)
CLCC Institut Curie
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), MLPA based techniques

GERMANY

Bayern
MÜNCHEN

Accreditation
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Medizinisch Genetisches Zentrum München
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
ULM

Accreditation
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Ulm
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

GERMANY

Bayern
WÜRZBURG

Accreditation
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universität Würzburg - Biozentrum
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
Molecular cytogenetic diagnosis of soft tissue sarcomas
University Hospitals Leuven - Gasthuisberg
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics

AUSTRALIA

Victoria
MELBOURNE

Accreditation
Molecular diagnosis of atypical teratoid rhabdoid tumor (SMARCB1 gene: full mutation screen and MLPA)
Monash Health
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Technique(s) : MLPA based techniques

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Rhabdoid Tumor (SMARCB1 FISH)
The Hospital for Sick Children
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of microdeletions/microduplications
Technique(s) : FISH

PORTUGAL

NORTE
PORTO

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

SPAIN

Andalucía
SEVILLA

Diagnosis of atypical teratoid rhabdoid tumor
Hospital Universitario Virgen del Rocío
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of microdeletions/microduplications
Technique(s) : FISH

FRANCE

AUVERGNE-RHONE-ALPES
LYON

Molecular diagnosis of rhabdoid tumor (SMARCB1 gene)
CHU de Lyon HCL - GH Edouard Herriot
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

CANADA

Alberta
CALGARY

Pediatric Cancer NGS Panel (12 genes)
Alberta Children's Hospital
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), PCR based techniques, MLPA based techniques, Array based techniques

GERMANY

Sachsen
DRESDEN

Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Carl Gustav Carus an der TU Dresden
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

FRANCE

BRETAGNE
BREST

Diagnosis of intellectual disability (Panel)
CHRU de Brest - Hôpital Morvan
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)

GERMANY

Nordrhein-Westfalen
BONN

Histopathological, molecular and cell biological analysis of tumor biopsies of the nervous system
Universitätsklinikum Bonn
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics, Pathology

GERMANY

Nordrhein-Westfalen
DÜSSELDORF

Histopathological, molecular and cell biological analysis of tumor biopsies of the nervous system
Universitätsklinikum Düsseldorf
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Molecular genetics, Pathology

ITALY

LIGURIA
GENOVA

Molecular diagnosis of rhabdoid tumor (SMARCB1 gene)
IRCCS Istituto G. Gaslini - Ospedale Pediatrico
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics

AUSTRIA

WIEN
WIEN

Molecular diagnosis of rhabdoid tumors (SMARCB1 gene)
Allgemeines Krankenhaus der Stadt Wien
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of rhabdoid tumor (tumoral tissue)
Centre hospitalier Sainte-Anne
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Pathology