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

Hamburg
HAMBURG
Molecular diagnosis of CVID / TACI related IgA deficiency (TNFRSF13B gene)
Labor Lademannbogen
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Hamburg
HAMBURG
Molecular diagnosis of Hypogammaglobulinemia due to CD19 deficiency (CD19 gene)
Labor Lademannbogen
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Mecklenburg-Vorpommern
ROSTOCK
Molecular diagnosis of ICOS deficiency
Centogene AG
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Cataluña
L'HOSPITALET DE LLOBREGAT
Molecular diagnosis of common variable immunodeficiency (TNFRSF13B, ICOS genes / sequence analysis entire coding region)
Reference Laboratory Genetics
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region

Bayern
MÜNCHEN
Molecular diagnosis of CVID (CD19, CD81, ICOS, MS4A1, TNFRSF13B, TNFRSF13C genes)
Pränatalmedizin München
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Cataluña
L'HOSPITALET DE LLOBREGAT
Diagnosis of primary immunodeficiency (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)

Baden-Württemberg
ULM
Molecular diagnosis of CVID (CD19, CD81, ICOS, TNFRSF13B, TNFRSF13C 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

ILE-DE-FRANCE
PARIS
Molecular diagnosis of common variable immunodeficiency (TNFRSF13B, CD19, MS4A1, TNFRSF13C genes)
CHU Paris - Hôpital Necker-Enfants Malades
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
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, PCR based techniques

Zuid-Holland
ROTTERDAM
Molecular diagnosis of Common Variable Immunodeficiency type 3 (CD19 gene)
Erasmus MC, Faculteitsgebouw
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Zuid-Holland
ROTTERDAM
Molecular diagnosis of Common Variable Immunodeficiency type 2 (TACI gene)
Erasmus MC, Faculteitsgebouw
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Zuid-Holland
ROTTERDAM
Molecular diagnosis of Common Variable Immunodeficiency type 4 (BAFFR gene)
Erasmus MC, Faculteitsgebouw
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Zuid-Holland
ROTTERDAM
Molecular diagnosis of Common Variable Immunodeficiency type 6 (CD81 gene)
Erasmus MC, Faculteitsgebouw
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Utrecht
UTRECHT
Diagnosis of Common Variable Immunodeficiency (Titers of anti-polysaccharide antibodies before and after vaccination)
UMC Utrecht - Universitair Medisch Centrum Utrecht
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Immunology

ILE-DE-FRANCE
PARIS
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)

Baden-Württemberg
TÜBINGEN
Molecular diagnosis of antibody deficiencies (NGS panel, 29 genes)
CeGaT GmbH
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Cataluña
BARCELONA
Molecular diagnosis of immunodeficiency, common variable (TACI gene)
Hospital Clínic de Barcelona
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

ILE-DE-FRANCE
PARIS
Molecular diagnosis of common variable immunodeficiency (CD19, CD79A, ICOS, TNFRSF13B, TNFRSF13C genes)
CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Cataluña
BARCELONA
Molecular diagnosis of common variable immunodeficiency due to an intrinsic B cell defect (CD81 and CD19 genes)
Hospital Clínic de Barcelona
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Cataluña
BARCELONA
Molecular diagnosis of common variable immunodeficiency due to TNFR deficiency (TNFRSF13C gene)
Hospital Clínic de Barcelona
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Sachsen
DRESDEN
Molecular diagnosis of CVID / TACI related IgA deficiency (TNFRSF13B gene)
Gemeinschaftspraxis für Humangenetik
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Sachsen
DRESDEN
Molecular diagnosis of ICOS deficiency
Gemeinschaftspraxis für Humangenetik
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Andalucía
MÁLAGA
Molecular diagnosis of common variable immunodeficiency (TNFRSF13B, ICOS genes)
Genetaq
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

NORTE
PORTO
Molecular diagnosis of common variable immunodeficiency (ICOS gene: sequencing of the entire coding region)
CGC Genetics / Centro de Genética Clínica
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region

Comunidad Valenciana
PATERNA
Molecular diagnosis of hydrolethalus (ICOS gene / complete sequencing)
IMEGEN - Instituto de Medicina Genómica
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, Whole Exome Sequencing (WES)

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)

Comunidad Valenciana
ELCHE
Diagnosis of common variable immunodeficiency (ICOS gene)
Bioarray
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

Észak-Magyarország
DEBRECEN
Molecular diagnosis of common variable immunodeficiency (ICOS and TACI genes)
University of Debrecen
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

Cataluña
BARCELONA
Diagnosis of primary immunodeficiency disorders
Hospital Universitari General Vall d'Hebron
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Immunology

Berlin
BERLIN
Immunological diagnosis of CVID
Charité - Universitätsmedizin Berlin (CVK)
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Immunology

ATTIKI
ATHENS
Diagnosis of familial common variable immunodeficiency by immunophenotyping and nephelometry
"Aghia Sophia" Children's Hospital
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Immunology

Niedersachsen
HANNOVER
Immunological diagnosis of familial common variable immunodeficiency (IgG, IgA, IgM, IgG subclasses, flow cytometry)
Medizinische Hochschule Hannover
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Immunology

Limburg
MAASTRICHT
Biochemical diagnosis of T-cell, B-cell and Severe Combined Immunodeficiency (Analyte: Adenosine Deaminase)
AZM - Academisch Ziekenhuis Maastricht
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Biochemical genetics
Objective(s)
: Analyte / Enzyme assay

LARISA
LARISSA
Molecular diagnosis of common variable immunodeficiency (Long-term PCR analysis of exons 2-3 of ICOS gene; sequencing of TNFRSF13B gene)
University of Thessaly (UTH)
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Technique(s)
: PCR based techniques

Madrid
SAN SEBASTIÁN DE LOS REYES
Diagnosis of common variable immunodeficiency due to TNFR deficiency (TNFRSF13B gene)
Laboratorio de Genética Clínica, S.L.
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

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

EMILIA ROMAGNA
BOLOGNA
Molecular diagnosis of common variable immunodeficiency (TNFRSF13B, TNFRSF13C, ICOS genes)
Policlinico S. Orsola-Malpighi - Area S. Orsola
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

Madrid
SAN SEBASTIÁN DE LOS REYES
Diagnosis of common variable immunodeficiency (CD19, CD81 genes)
Laboratorio de Genética Clínica, S.L.
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

Madrid
SAN SEBASTIÁN DE LOS REYES
Diagnosis of common variable immunodeficiency (ICOS, MS4A1 genes)
Laboratorio de Genética Clínica, S.L.
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

Madrid
SAN SEBASTIÁN DE LOS REYES
Diagnosis of common variable immunodeficiency due to TNFR deficiency (TNFRSF13B, TNFRSF13C genes)
Laboratorio de Genética Clínica, S.L.
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

OOST-VLAANDEREN
GENT
Molecular diagnosis of CVID (common variable immunodeficiency) (gene analysis for ICOS, TNFRSF13B, TNFRSF13C, CD19, CD81, CR2, MS4A1, PRKCD, PLCG2, PIK3CD, PIK3R1, IL21, IL21R, NFKB1, NFKB2, LRBA, CTLA4, VAV1, RAC2, BLK, BTK, IGHM, CD79A, CD79B, IGLL1, BLNK, TCF7L1 , CD40LG, CD40, AICDA, UNG, using whole exome sequencing)
Ghent University Hospital - UZGent
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Whole Exome Sequencing (WES)

TOSCANA
FIRENZE
Molecular diagnosis of common variable immunodeficiency (ICOS gene)
Azienda Ospedaliera Universitaria Anna Meyer
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
Technique(s)
: Sanger sequencing

WIEN
WIEN