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Caption : Accreditation =Accreditation ;

UNITED KINGDOM

South Glamorgan
CARDIFF

Accreditation Molecular analysis of the TNFRSF13B gene in immunodeficiency syndromes (test under development)
University Hospital of Wales
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

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GERMANY

Hamburg
HAMBURG

Accreditation 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
Technical procedure(s) : Sanger sequencing

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GERMANY

Hamburg
HAMBURG

Accreditation 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
Technical procedure(s) : Sanger sequencing

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GERMANY

Mecklenburg-Vorpommern
ROSTOCK

Accreditation Molecular diagnosis of ICOS deficiency
Centogene AG
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

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SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation 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

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GERMANY

Bayern
MÜNCHEN

Accreditation 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
Technical procedure(s) : Sanger sequencing

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GERMANY

Baden-Württemberg
ULM

Accreditation 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
Technical procedure(s) : Sanger sequencing

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NETHERLANDS

Zuid-Holland
ROTTERDAM

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

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NETHERLANDS

Zuid-Holland
ROTTERDAM

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

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NETHERLANDS

Zuid-Holland
ROTTERDAM

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

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NETHERLANDS

Zuid-Holland
ROTTERDAM

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

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NETHERLANDS

Utrecht
UTRECHT

Accreditation 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

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SPAIN

Cataluña
BARCELONA

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

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SPAIN

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

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SPAIN

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

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GERMANY

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
Technical procedure(s) : Sanger sequencing

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GERMANY

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
Technical procedure(s) : Sanger sequencing

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SPAIN

Andalucía
MÁLAGA

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

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PORTUGAL

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

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SPAIN

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
Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing, Whole Exome Sequencing (WES)

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FRANCE

NORD-PAS-DE-CALAIS
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
Technical procedure(s) : NGS sequencing (except WES)

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SPAIN

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
Technical procedure(s) : NGS sequencing (except WES)

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HUNGARY

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
Technical procedure(s) : Sanger sequencing

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SPAIN

Cataluña
BARCELONA

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

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GERMANY

Berlin
BERLIN

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

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GREECE

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

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GERMANY

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

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NETHERLANDS

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

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GREECE

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
Technical procedure(s) : PCR based techniques

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FRANCE

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) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
Technical procedure(s) : Sanger sequencing

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FRANCE

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
Technical procedure(s) : Sanger sequencing

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SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Molecular diagnosis of common variable immunodeficiency due to TNFR deficiency (TNFRSF13B gene: entire coding sequence)
Laboratorio de Genética Clínica, S.L.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region

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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

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ITALY

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

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SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Molecular diagnosis of common variable immunodeficiency due to an intrinsic B cell defect (CD19 and CD81 genes: entire coding sequence)
Laboratorio de Genética Clínica, S.L.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region

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SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Molecular diagnosis of common variable immunodeficiency due to an intrinsic T cell defect (ICOS and MS4A1 genes: entire coding sequence)
Laboratorio de Genética Clínica, S.L.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region

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SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Molecular diagnosis of common variable immunodeficiency due to TNFR deficiency (TNFRSF13B and TNFRSF13C genes: entire coding sequence)
Laboratorio de Genética Clínica, S.L.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region

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BELGIUM

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
Technical procedure(s) : Whole Exome Sequencing (WES)

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FRANCE

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
Technical procedure(s) : NGS sequencing (except WES)

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ITALY

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
Technical procedure(s) : Sanger sequencing

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