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Caption : Accreditation =Accreditation
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NETHERLANDS

Groningen
GRONINGEN

Accreditation
Molecular diagnosis of Epidermolysis Bullosa Simplex (KRT5 and KRT14 gene)
UMCG - Universitair Medisch Centrum Groningen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
FREIBURG

Accreditation
Molecular diagnosis of epidermolysis bullosa (genes: COL7A1, COL17A1, ITGB4, ITGA6, KRT5, KRT14, LAMB3, LAMC2 and LAMA3)
Praxis für Humangenetik Freiburg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

NETHERLANDS

Groningen
GRONINGEN

Accreditation
Diagnosis of Epidermolysis Bullosa (Immunofluorescence and electron microscopy analysis of skin biopsies)
UMCG - Universitair Medisch Centrum Groningen
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Biochemical genetics
Objective(s) : Protein expression
Technique(s) : Immunohistochemistry

GERMANY

Rheinland-Pfalz
INGELHEIM AM RHEIN

Accreditation
Molecular diagnosis of basal epidermolysis bullosa simplex (KRT5, KRT14 genes)
Bioscientia Institut für Medizinische Diagnostik GmbH
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Molecular diagnosis of basal epidermolysis bullosa simplex (KRT5, KRT14 genes)
Reference Laboratory Genetics
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
TÜBINGEN

Accreditation
Molecular diagnosis of KRT5 gene associated epidermolysis bullosa simplex
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 basal epidermolysis bullosa simplex (ITGB4, KRT5, KRT14, PLEC genes)
Pränatalmedizin München
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

UNITED KINGDOM

Tayside
DUNDEE

Accreditation
Molecular diagnosis of Epidermolysis Bullosa Simplex (KRT5 & KRT14 genes)
Ninewells Hospital and Medical School
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ITALY

LAZIO
ROMA

DENMARK

Jylland
AARHUS

Molecular diagnosis of epidermolysis bullosa (KRT5 and KRT14 gene)
Aarhus Universitetshospital - Skejby
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : Sanger sequencing

POLAND

Warszawa
WARSZAWA

Molecular diagnosis of junctional epidermolysis bullosa (LAMB3, LAMC2, LAMA3 and COL17A1 gene)
Instytut Matki i Dziecka
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

POLAND

Warszawa
WARSZAWA

Molecular diagnosis of simplex epidermolysis bullosa (KRT5 and KRT14 genes)
Instytut Matki i Dziecka
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) : Sanger sequencing

GERMANY

Nordrhein-Westfalen
BONN

Molecular diagnosis of KRT5 gene associated hyperpigmentation anomalies
Universitätsklinikum Bonn
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

SPAIN

Comunidad Valenciana
PATERNA

Molecular diagnosis of basal epidermolysis bullosa simplex (KRT14, KRT5, PLEC1 genes)
IMEGEN - Instituto de Medicina Genómica
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Comunidad Valenciana
PATERNA

Molecular diagnosis of basal epidermolysis bullosa simplex (KRT5, KRT14 genes)
Sistemas Genómicos S.L.
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Comunidad Valenciana
SANT JOAN D'ALACANT

Molecular diagnosis of basal epidermolysis bullosa simplex (KRT5, KRT14 genes / sequencing)
Centro Inmunológico de Alicante (CIALAB)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Castilla - León
SALAMANCA

Molecular diagnosis of basal epidermolysis bullosa simplex (KRT5 gene / sequencing)
Universidad de Salamanca. Facultad de Medicina
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

PORTUGAL

NORTE
PORTO

Molecular diagnosis of Epidermolysis bullosa simplex (KRT5 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

GERMANY

Baden-Württemberg
STUTTGART

Molecular diagnosis of basal epidermolysis bullosa simplex (KRT5, KRT14 genes)
Klinikum Stuttgart - Standort Olgahospital
Purpose(s) : Antenatal diagnosis, 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

Baden-Württemberg
FREIBURG

Molecular diagnosis of basal epidermolysis bullosa simplex (DST, EXPH5, ITGB4, KRT5, KRT14, PLEC genes)
Institut für Humangenetik am Universitätsklinikum Freiburg
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

FRANCE

ILE-DE-FRANCE
PARIS

Typing of epidermolysis bullosa (immunohistochemistry, electronic microscopy on skin biopsy)
CHU Paris - Hôpital Necker-Enfants Malades
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Biochemical genetics
Objective(s) : Protein expression
Technique(s) : Immunohistochemistry

SWITZERLAND

Suisse Romande
LAUSANNE

Diagnosis of Epidermolysis bullosa by antigen mapping
Centre Hospitalier Universitaire Vaudois CHUV - Hôpital Beaumont -
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Immunology

ITALY

LAZIO
ROMA

Molecular diagnosis of epidermolysis bullosa intraepidermic (KRT5 gene)
Istituto Dermopatico dell'Immacolata - IRCCS
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

UNITED KINGDOM

Greater London
LONDON

Diagnostic testing of Epidermolysis Bullosa using electron microscopy of skin biopsy samples
St Thomas' Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Pathology

UNITED KINGDOM

Greater London
LONDON

Diagnostic testing of Epidermolysis Bullosa using immunofluorescence microscopy antigen mapping of skin biopsy samples
St Thomas' Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Biochemical genetics
Objective(s) : Protein expression
Technique(s) : Immunohistochemistry

UNITED KINGDOM

Greater London
LONDON

Molecular diagnosis of Epidermolysis Bullosa (mutation screening of the COL7A1, ITGA6, ITGB4, LAMA3, LAMB3 & LAMC2 genes)
St Thomas' Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons

HUNGARY

Közép-Magyarország
BUDAPEST

Molecular diagnosis of epidermolysis bullosa (COL7A1, KRT5 and KRT14 genes)
Department of Dermatology, Venereology and Dermatoncology, Semmelweis University
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ISRAEL

ISRAEL
HAIFA

Molecular diagnosis of Epidermolysis Bullosa Lethalis (LAMC2, LAMB3, Linkage analysis)
The Bnai Zion Medical Center, Technion-Rappaport Faculty of Medicine
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

ISRAEL

ISRAEL
HAIFA

Molecular diagnosis of Epidermolysis Bullosa Dystrophic (COL7A1, Linkage analysis)
The Bnai Zion Medical Center, Technion-Rappaport Faculty of Medicine
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

CZECH REPUBLIC

South Moravia
BRNO

Molecular diagnosis of epidermolytic epidermolysis bullosa (KRT5 and KRT14 genes)
University hospital Brno
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of basal epidermolysis bullosa simplex (COL7A1, KRT5, KRT14, PLEC genes)
Laboratorio de Genética Clínica, S.L.
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

GERMANY

Baden-Württemberg
HEIDELBERG

Electron microscopic diagnosis of hereditary epidermolysis bullosa
Universitäts-Hautklinik Heidelberg
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Pathology

SPAIN

Madrid
MAJADAHONDA

Molecular diagnosis of basal epidermolysis bullosa simplex (sequencing of KRT5 and KRT14 genes)
Genyca Innova
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

GERMANY

Baden-Württemberg
FREIBURG

Electron microscopy and immunofluorescence mapping of epidermolysis bullosa
Universitäts-Klinik für Dermatologie und Venerologie
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Biochemical genetics
Objective(s) : Protein expression
Technique(s) : Immunohistochemistry

GERMANY

Baden-Württemberg
FREIBURG

Molecular diagnosis of basal epidermolysis bullosa simplex (DST, KRT14, KRT5 genes)
Universitäts-Klinik für Dermatologie und Venerologie
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

AUSTRIA

SALZBURG
SALZBURG

Molecular diagnosis of epidermolytic epidermolysis bullosa (KRT5, KRT14, PLEC1, and FERMT1 gene)
Salzburger Landeskliniken (SALK) / Paracelsus Med. Privatuniversität (PMU)
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Comunidad Valenciana
PATERNA

Preimplantation genetic diagnosis of basal epidermolysis bullosa simplex (KRT5 gene)
Igenomix Spain
Purpose(s) : Pre-implantation diagnosis
Specialty(ies) : Molecular genetics

SPAIN

Madrid
MADRID

Diagnosis of epidermolysis bullosa simplex (KRT14, KRT5 genes)
CIEMAT - Centro de Investigaciones Energéticas Medioambientales y Tecnológicas
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing

HUNGARY

Dél-Alföld
SZEGED

Epidermolysis bullosa
University of Szeged Deparment of Medical Genetics
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Sanger sequencing