Search for a diagnostic test
21 Result(s)
Caption
: Accreditation
= ;

FRANCE
ILE-DE-FRANCE
PARIS
Diagnosis of X-linked thombocytopenia
CHU Paris - Hôpital Robert Debré
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Hematology

FRANCE
ILE-DE-FRANCE
PARIS
Diagnosis of X-linked thombocytopenia
AP-HP.Sorbonne Université - Hôpital d'Enfants Armand-Trousseau
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Hematology

FRANCE
ILE-DE-FRANCE
ARGENTEUIL
Diagnosis of congenital deficiency of coagulation factors
Centre hospitalier Victor Dupouy
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Hematology

GERMANY
Bayern
MARTINSRIED/PLANEGG
Diagnosis of X-linked Thrombocytopenia (WAS gene)
MVZ Martinsried GmbH
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

SWITZERLAND
Suisse Romande
GENÈVE
Diagnosis of platelets disorders
Hôpitaux Universitaires de Genève HUG
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Hematology

SPAIN
Cataluña
L'HOSPITALET DE LLOBREGAT
Diagnosis of thrombocytopenia related disorders (gene panel)
Reference Laboratory Genetics
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES), Sanger sequencing

FRANCE
ILE-DE-FRANCE
PARIS
Diagnosis of thrombopathies (Panel)
CHU Paris - Hôpital Robert Debré
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES), Sanger sequencing

GERMANY
Bayern
MÜNCHEN
Diagnosis of hereditary thrombocytopenia with normal platelets (CYCS, MASTL, WAS genes)
Pränatal-Medizin München MVZ GmbH
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

FRANCE
ILE-DE-FRANCE
PARIS
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
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
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
VLAAMS BRABANT
LEUVEN
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)

BELGIUM
LIEGE
LIEGE
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)

DENMARK
Hovedstaden
COPENHAGEN
Molecular diagnosis of X-linked thrombocytopenia (WAS gene)
Rigshospitalet
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

GERMANY
Niedersachsen
OSNABRÜCK
Diagnosis of X-linked Thrombocytopenia (WAS gene)
Praxis Dres. Gencik
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

GERMANY
Mecklenburg-Vorpommern
ROSTOCK
Diagnosis of thrombocytopenias (NGS Screening Panel, 14 genes)
CENTOGENE GmbH
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES), Sanger sequencing

FRANCE
PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
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
GRAND-EST
VANDOEUVRE-LÈS-NANCY
Diagnosis of X-linked thombocytopenia
CHU de Nancy - Hôpitaux de Brabois
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Hematology

CZECH REPUBLIC
South Moravia
BRNO
Prenatal and postnatal molecular diagnosis of X-linked thrombocytopenia (WAS gene)
Center for cardiovascular surgery and transplantation
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis
Specialty(ies)
: Molecular genetics

SERBIA
Serbia
BELGRADE
Diagnosis of inherited bleeding disorders (hemophilia, von Willebrand disease and others rare bleeding disorders)
Blood Transfusion Institute of Serbia
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Hematology

AUSTRIA
WIEN
WIEN