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FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of X-linked thombocytopenia
CHU Paris - Hôpital Robert Debré

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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FRANCE

ILE-DE-FRANCE
PARIS

Diagnosis of X-linked thombocytopenia
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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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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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

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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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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

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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

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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) : Sequence analysis: entire coding region

Technique(s) : NGS sequencing (except WES)

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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

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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

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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)

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GERMANY

Mecklenburg-Vorpommern
GREIFSWALD

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)

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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)

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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)

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DENMARK

Hovedstaden
COPENHAGEN

Molecular diagnosis of X-linked thrombocytopenia (WAS gene)
Rigshospitalet

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Molecular genetics

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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

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GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Diagnosis of thrombocytopenias (NGS Screening Panel, 14 genes)
Centogene AG

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

GRAND-EST
VANDOEUVRE-LÈS-NANCY

Diagnosis of X-linked thombocytopenia
CHU de Nancy - Hôpitaux de Brabois

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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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

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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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AUSTRIA

WIEN
WIEN

Molecular diagnosis of isolated constitutional thrombocytopenia (ACTN1, CYCS, GATA1, ITGB3, MASTL, TUBB1, and WAS genes)
Praxis für Humangenetik

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Molecular genetics

Objective(s) : Sequence analysis: entire coding region

Technique(s) : Sanger sequencing

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21 Result(s)

Filter by

Speciality(ies)/objective(s)

Technique(s)

Purpose(s)

Quality management

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Diagnosis of X-linked thombocytopenia
CHU Paris - Hôpital Robert Debré

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

Diagnosis of X-linked thombocytopenia
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

Diagnosis of congenital deficiency of coagulation factors
Centre hospitalier Victor Dupouy

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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

Diagnosis of platelets disorders
Hôpitaux Universitaires de Genève HUG

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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

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

Technique(s) : NGS sequencing (except WES)

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)

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)

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)

Molecular diagnosis of X-linked thrombocytopenia (WAS gene)
Rigshospitalet

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Molecular genetics

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

Diagnosis of thrombocytopenias (NGS Screening Panel, 14 genes)
Centogene AG

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 X-linked thombocytopenia
CHU de Nancy - Hôpitaux de Brabois

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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

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

21 Result(s)

Filter by

Speciality(ies)/objective(s)

Technique(s)

Purpose(s)

Quality management

Country(ies)

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

Diagnosis of X-linked thombocytopenia CHU Paris Est - Hôpital d'Enfants Armand-Trousseau Purpose(s) : Post-natal diagnosis Specialty(ies) : Hematology

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

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

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

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

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 Technique(s) : NGS sequencing (except WES)

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)

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)

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)

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

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

Diagnosis of thrombocytopenias (NGS Screening Panel, 14 genes) Centogene AG 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 X-linked thombocytopenia CHU de Nancy - Hôpitaux de Brabois Purpose(s) : Post-natal diagnosis Specialty(ies) : Hematology

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

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 X-linked thombocytopenia
CHU Paris - Hôpital Robert Debré

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

Diagnosis of X-linked thombocytopenia
CHU Paris Est - Hôpital d'Enfants Armand-Trousseau

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

Diagnosis of congenital deficiency of coagulation factors
Centre hospitalier Victor Dupouy

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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

Diagnosis of platelets disorders
Hôpitaux Universitaires de Genève HUG

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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

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

Technique(s) : NGS sequencing (except WES)

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)

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)

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)

Molecular diagnosis of X-linked thrombocytopenia (WAS gene)
Rigshospitalet

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Molecular genetics

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

Diagnosis of thrombocytopenias (NGS Screening Panel, 14 genes)
Centogene AG

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 X-linked thombocytopenia
CHU de Nancy - Hôpitaux de Brabois

Purpose(s) : Post-natal diagnosis

Specialty(ies) : Hematology

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

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