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UNITED KINGDOM

Greater London
LONDON

Accreditation
Molecular diagnosis of X-linked Lymphoproliferative disease (SAP and XIAP genes)
Great Ormond Street Hospital for Children, York House
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

NETHERLANDS

Zuid-Holland
LEIDEN

Accreditation
Molecular diagnosis of X-linked Lymphoproliferative Disease (SH2D1A gene)
LUMC - Leids Universitair Medisch Centrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation
Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene)
Centogene AG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

IRELAND

County Dublin
DUBLIN

Accreditation
Molecular cytogenetic diagnosis of Lymphoma and Lymphoproliferative diseases (by FISH and occasionally by conventional karyotyping)
Our Lady's Children's Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : FISH, Karyotyping

UNITED KINGDOM

South Glamorgan
CARDIFF

Accreditation
Molecular cytogenetic diagnostic of Lymphoma and Lymphoproliferative disorders (by conventional karyotyping and FISH)
University Hospital of Wales
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

UNITED KINGDOM

Nottinghamshire
NOTTINGHAM

Accreditation
Molecular cytogenetic diagnostic of Lymphoma and Lymphoproliferative diseases (by karyotyping and FISH)
Nottingham City Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

UNITED KINGDOM

Wiltshire
SALISBURY

Accreditation
Cytogenetic and molecular cytogenetic diagnostic of Lymphoma and Lymphoproliferative diseases (SH2D1A, FAS & XIAP genes)
Salisbury District Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics

UNITED KINGDOM

Tyne & Wear
NEWCASTLE UPON TYNE

Accreditation
Cytogenetic diagnostic of Lymphoma and Lymphoproliferative diseases
Newcastle upon Tyne Hospitals NHS Trust
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

West Midlands
BIRMINGHAM

Accreditation
Molecular diagnosis of Lymphoma and Lymphoproliferative disorders (TCRB and TCRG PCR for B and T cell clonality studies)
Birmingham Women's NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

UNITED KINGDOM

Merseyside
LIVERPOOL

Accreditation
Molecular cytogenetic diagnosis of Lymphoma and Lymphoproliferative diseases (by FISH analysis and conventional cytogenetics)
Liverpool Women's NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

UNITED KINGDOM

Lanarkshire
GLASGOW

Accreditation
Cytogenetic diagnostic of Lymphoma and Lymphoproliferative diseases
Southern General Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

NETHERLANDS

Utrecht
UTRECHT

Accreditation
Molecular diagnosis of X-linked Lymphoproliferative Syndrome type 1 and 2 (SH2D1A and XIAP gene)
UMC Utrecht - Universitair Medisch Centrum Utrecht
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

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation
Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene: sequencing / MLPA)
Diagenom GmbH
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

UNITED KINGDOM

Greater London
LONDON

Accreditation
Molecular cytogenetic diagnostic of Lymphoma and Lymphoproliferative diseases (by FISH analysis)
King's College Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

UNITED KINGDOM

West Yorkshire
LEEDS

Accreditation
Cytogenetic diagnostic of Lymphoma and Lymphoproliferative disorders (by karyotyping)
St James's University Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

Avon
BRISTOL

Accreditation
Molecular cytogenetic diagnostic of Lymphoma and Lymphoproliferative disorders (by FISH analysis)
Southmead Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : FISH

UNITED KINGDOM

Greater London
LONDON

Accreditation
Molecular diagnosis of X-linked Lymphoproliferative disease type 2 (XIAP gene)
Great Ormond Street Hospital for Children, York House
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
MANNHEIM

Accreditation
Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene)
Zentrum für Humangenetik Mannheim
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

UNITED KINGDOM

South Yorkshire
SHEFFIELD

Accreditation
Molecular cytogenetic diagnostic of Lymphoma and Lymphoproliferative diseases (CLL Panel, TP53, CCND1, BCL2, BCL6: by FISH)
Sheffield Children's NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene)
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

UNITED KINGDOM

Greater London
LONDON

Accreditation
Molecular diagnosis of X-linked Lymphoproliferative Syndrome type 1 (SH2D1A and XIAP genes: Sequencing of the entire coding region of gene (s) / Testing for known mutations in family members)
Great Ormond Street Hospital for Children, York House
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of agammaglobulinemia (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)

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Hemophagocytic Lymphohistiocytosis NGS Panel and Del/Dup Analysis (14 genes)
The Hospital for Sick Children and University of Toronto
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Array based techniques

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of primary hemophagocytic lymphohistiocytosis (PRF1, UNC13D, STX11, STXBP2, SH2D1A, RAB27A genes)
Reference Laboratory Genetics
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), MLPA based techniques

GERMANY

Baden-Württemberg
TÜBINGEN

Accreditation
Molecular diagnosis of X-linked lymphoproliferative disease (XIAP gene)
CeGaT GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

GERMANY

Bayern
MÜNCHEN

Accreditation
Molecular diagnosis of X-linked lymphoproliferative disease (ITK, SH2D1A and XIAP genes)
Pränatalmedizin München
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : Sanger sequencing, MLPA based techniques

UNITED KINGDOM

Wiltshire
SALISBURY

Accreditation
Molecular Cytogenetic diagnosis of X-linked Lymphoproliferative disease (FISH of SH2D1a at Xq25)
Salisbury District Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Technique(s) : FISH

DENMARK

Fyn
ODENSE

Accreditation
Molecular diagnosis of X-linked lymphoproliferative disease
Odense University hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
ULM

Accreditation
Molecular diagnosis of X-linked lymphoproliferative disease (ITK, SH2D1A and XIAP genes)
DRK Baden-Württemberg/ Hessen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Molecular diagnosis of X-linked lymphoproliferative disease (XIAP and SH2D1A genes)
CHU Paris - Hôpital Necker-Enfants Malades
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : NGS sequencing (except WES), Sanger sequencing, PCR based techniques, MLPA based techniques

NETHERLANDS

Zuid-Holland
ROTTERDAM

Accreditation
Molecular diagnosis of X-linked Lymphoproliferative Syndrome (SH2D1A and XIAP gene)
Erasmus MC, Faculteitsgebouw
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
SINGEN /HTWL.

Accreditation
Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A and XIAP genes)
Institut für Laboratoriumsmedizin und Humangenetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

NETHERLANDS

Utrecht
UTRECHT

Accreditation
Diagnosis of X-linked Lymphoproliferative Disease type 1 (Intracellular expression of SAP)
UMC Utrecht - Universitair Medisch Centrum Utrecht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

NETHERLANDS

Utrecht
UTRECHT

Accreditation
Diagnosis of X-linked Lymphoproliferative Disease type 2 (Intracellular expression of XIAP)
UMC Utrecht - Universitair Medisch Centrum Utrecht
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of hereditary immune deficiencies (Panel)
CHU Paris - Hôpital Necker-Enfants Malades
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)

DENMARK

Hovedstaden
COPENHAGEN

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene)
Rigshospitalet
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

LAZIO
ROMA

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene)
Laboratorio Genoma
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Oxfordshire
OXFORD

Cytogenetic diagnostic of Lymphoma and Lymphoproliferative diseases
The Churchill Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

Tayside
DUNDEE

Cytogenetic diagnostic of Lymphoma and Lymphoproliferative diseases
Ninewells Hospital and Medical School
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : Karyotyping

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

Molecular cytogenetic diagnostic of Lymphoma and Lymphoproliferative diseases (by FISH analysis)
Addenbrooke's Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

UNITED KINGDOM

Greater London
LONDON

Cytogenetic and molecular cytogenetic diagnosis of Lymphoma and Lymphoproliferative diseases (by G-banded karyotyping and FISH analysis)
Barts Health NHS trust - The Royal London Hospital-Pathology Pharmacy Building
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

UNITED KINGDOM

Antrim and Newtownabbey
BELFAST

Molecular cytogenetic diagnostic of Lymphoma and Lymphoproliferative disorders (by FISH analysis)
Belfast City Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

UNITED KINGDOM

Greater Manchester
MANCHESTER

Molecular cytogenetic diagnostic of Lymphoma and Lymphoproliferative disorders (by FISH analysis)
Christie Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

GERMANY

Niedersachsen
OSNABRÜCK

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene)
Praxis Dres. Gencik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

SPAIN

Cataluña
BARCELONA

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A and XIAP genes)
Hospital Clínic de Barcelona
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Comunidad Valenciana
PATERNA

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A and XIAP genes)
IMEGEN - Instituto de Medicina Genómica
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

País Vasco
DERIO

Molecular diagnosis of X-linked lymphoproliferative disease (aCGH)
Genetadi Biotech S.L.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

West Yorkshire
LEEDS

Molecular cytogenetic diagnostic of Lymphoma and Lymphoproliferative disorders (by FISH analysis)
St James's Institute of Oncology
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

UNITED KINGDOM

Dorset
BOURNEMOUTH

Molecular cytogenetic diagnostic of Lymphoma and Lymphoproliferative disorders (by FISH analysis)
Royal Bournemouth Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

SPAIN

Cataluña
BARCELONA

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene)
Hospital del Mar
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Comunidad Valenciana
ELCHE

Diagnosis of X-linked lymphoproliferative disease (SH2D1A, XIAP gene)
Bioarray
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

FRANCE

HAUTS-DE-FRANCE
LILLE

Diagnosis of inflammatory bowel disease (Panel)
CHRU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
Technique(s) : NGS sequencing (except WES)

HUNGARY

Észak-Magyarország
DEBRECEN

Molecular diagnosis of X-linked lymphoproliferative syndrome (SH2D1A and XIAP gene)
University of Debrecen
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

ITALY

LOMBARDIA
BRESCIA

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A, XIAP genes)
Azienda Ospedaliera Spedali Civili di Brescia
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

EMILIA ROMAGNA
BOLOGNA

Molecular diagnosis of X-linked lymphoproliferative disease
Policlinico S. Orsola-Malpighi - Area S. Orsola
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

HUNGARY

Közép-Magyarország
DEBRECEN

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene)
University of Debrecen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GREECE

ATTIKI
ATHENS

Diagnosis of X-linked proliferative disease by immunophenotyping and flow cytometry
"Aghia Sophia" Children's Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene)
Albrecht-Kossel-Institute for Neuroregeneration (AKos)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

CZECH REPUBLIC

South Moravia
BRNO

Prenatal and postnatal molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene)
Center for cardiovascular surgery and transplantation
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics

SWEDEN

Stockholms läns landsting
STOCKHOLM

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1 gene)
Karolinska University Hospital - Clinical Genetics
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SLOVENIA

SLOVENIA
LJUBLJANA

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A and XIAP genes)
University Medical Centre Ljubljana
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
ULM

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A and XIAP genes)
Klinik für Kinder- und Jugendmedizin des Universitätsklinikums Ulm
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

ISRAEL

ISRAEL
PETAH TIKVA

Molecular diagnosis of X-linked lymphoproliferative disease (XIAP and SH2DA1 gene sequencing)
Schneider Children's Medical Center of Israel
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of X-linked lymphoproliferative disease (XIAP, SH2D1A genes)
Laboratorio de Genética Clínica, S.L.
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis, Pre-symptomatic 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, MLPA based techniques

SPAIN

Madrid
MADRID

Molecular diagnosis of X-linked lymphoproliferative disease (SH2D1A gene)
Centro Nacional de Investigaciones Oncológicas (CNIO)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
ULM

Immunological diagnosis of primary immunodeficiencies (PID) - Immunophenotyping including adhesion molecules
Klinik für Kinder- und Jugendmedizin des Universitätsklinikums Ulm
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

BELGIUM

OOST-VLAANDEREN
GENT

Immunochemical diagnosis of X-linked Lymphoproliferative disease (SAP and XIAP protein expression)
Ghent University Hospital - UZGent
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Biochemical genetics, Immunology
Objective(s) : Protein expression
Technique(s) : Immunohistochemistry