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Caption : Accreditation =Accreditation
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FRANCE

ILE-DE-FRANCE
ARGENTEUIL

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

FRANCE

CENTRE-VAL DE LOIRE
TOURS

Accreditation
Congenital fibrinogen deficiency and coagulation factors deficiency
CHRU de Tours - Hôpital Trousseau
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

FRANCE

AUVERGNE-RHONE-ALPES
SAINT-PRIEST-EN-JAREZ

Accreditation
Diagnosis of congenital fibrinogen deficiency and coagulation factors deficiency
CHU de Saint-Etienne - Hôpital Nord
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

UNITED KINGDOM

Greater London
LONDON

Accreditation
Molecular diagnosis of Combined Factor V and Factor VIII deficiency (MCFD2 and LMAN1 genes)
St Thomas' Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

FRANCE

ILE-DE-FRANCE
BOULOGNE-BILLANCOURT

Accreditation
Diagnosis of congenital fibrinogen deficiency and coagulation factors deficiency
CHU Paris IdF Ouest - Hôpital Ambroise Paré
Purpose(s) : Post-natal diagnosis
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) : Sanger sequencing, PCR based techniques

GERMANY

Bayern
MÜNCHEN

Accreditation
Diagnosis of combined factor V and factor VIII deficiency (LMAN1, MCFD2 genes)
Pränatalmedizin München
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : Sanger sequencing, MLPA based techniques

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of rare coagulation 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

IRELAND

County Dublin
DUBLIN

Accreditation
Diagnosis of Combined Deficiency of Factor V and Factor VIII
St James's Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Hematology

GERMANY

Nordrhein-Westfalen
BONN

Accreditation
Diagnosis of combined factor V and factor VIII deficiency (LMAN1, MCFD2 genes)
Universitätsklinikum Bonn (AöR)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

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)

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

SPAIN

Comunidad Valenciana
VALENCIA

Diagnosis of combined deficiency of factor V and factor VIII (LMAN1, MCFD2 genes)
Hospital Universitario y Politécnico La Fe
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

SPAIN

Comunidad Valenciana
VALENCIA

Diagnosis of combined deficiency of factor V and factor VIII (LMAN1, MCFD2 genes)
Hospital Universitario y Politécnico La Fe
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)