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SWITZERLAND

Suisse Romande
GENÈVE

Diagnosis of platelets disorders
Hôpitaux Universitaires de Genève HUG

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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GERMANY

Hamburg
HAMBURG

Molecular diagnosis of bleeding diathesis due to thromboxane synthesis deficiency (TBXA2R gene)
Labor Lademannbogen

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Molecular genetics

Objective(s) : Sequence analysis: entire coding region

Technique(s) : Sanger sequencing

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SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Diagnosis of rare hemorrhagic disorder due to a platelet anomaly (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

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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) : Mutation scanning/screening and sequence analysis of selected exons

Technique(s) : NGS sequencing (except WES)

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FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of hemorrhagic disorders due to a constitutional platelet anomaly (Panel)
CHU Paris Est - 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)

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FRANCE

ILE-DE-FRANCE
ARGENTEUIL

Diagnosis of congenital deficiency of coagulation factors
Centre hospitalier Victor Dupouy

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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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

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Diagnosis of platelets disorders
Hôpitaux Universitaires de Genève HUG

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

Molecular diagnosis of bleeding diathesis due to thromboxane synthesis deficiency (TBXA2R gene)
Labor Lademannbogen

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Molecular genetics

Objective(s) : Sequence analysis: entire coding region

Technique(s) : Sanger sequencing

Diagnosis of rare hemorrhagic disorder due to a platelet anomaly (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

Diagnosis of congenital deficiency of coagulation factors
Centre hospitalier Victor Dupouy

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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

Search for a diagnostic test

7 Result(s)

Filter by

Speciality(ies)/objective(s)

Technique(s)

Purpose(s)

Quality management

Country(ies)

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

Molecular diagnosis of bleeding diathesis due to thromboxane synthesis deficiency (TBXA2R gene) Labor Lademannbogen Purpose(s) : Post-natal diagnosis Specialty(ies) : Molecular genetics Objective(s) : Sequence analysis: entire coding region Technique(s) : Sanger sequencing

Diagnosis of rare hemorrhagic disorder due to a platelet anomaly (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

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

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

Diagnosis of platelets disorders
Hôpitaux Universitaires de Genève HUG

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

Molecular diagnosis of bleeding diathesis due to thromboxane synthesis deficiency (TBXA2R gene)
Labor Lademannbogen

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Molecular genetics

Objective(s) : Sequence analysis: entire coding region

Technique(s) : Sanger sequencing

Diagnosis of rare hemorrhagic disorder due to a platelet anomaly (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

Diagnosis of congenital deficiency of coagulation factors
Centre hospitalier Victor Dupouy

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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