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Caption : Accreditation =Accreditation
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SWITZERLAND

Suisse Romande
GENÈVE

Accreditation
Search of duplications and/or deletions by array-CGH
Hôpitaux Universitaires de Genève HUG

FRANCE

OCCITANIE
TOULOUSE

FRANCE

AUVERGNE-RHONE-ALPES
BRON

FRANCE

HAUTS-DE-FRANCE
LILLE

Accreditation
Diagnosis of inherited disorders of cholestasis (Panel)
CHRU de Lille - Centre de Biologie Pathologie Génétique

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

Accreditation
Diagnosis of metabolic diseases (gene panel)
Reference Laboratory Genetics

SPAIN

Cataluña
L'HOSPITALET DE LLOBREGAT

UNITED KINGDOM

Devon
EXETER

UNITED KINGDOM

South Yorkshire
SHEFFIELD

UNITED KINGDOM

Tyne & Wear
NEWCASTLE UPON TYNE

Accreditation
Biochemical diagnosis of Peroxisomal disorders (Analyte: Very Long Chain Fatty Acids)
The Great North Children's Hospita, Royal Victoria Infirmary

UNITED KINGDOM

Tyne & Wear
NEWCASTLE UPON TYNE

Accreditation
Biochemical diagnosis of Peroxisomal disorders (Analyte: Pristanic acid)
The Great North Children's Hospita, Royal Victoria Infirmary

FRANCE

ILE-DE-FRANCE
PARIS

Peroxysomal diseases testing
CHU Paris - Hôpital Necker-Enfants Malades

SPAIN

País Vasco
BARAKALDO

SPAIN

Madrid
CANTOBLANCO

SPAIN

Comunidad Valenciana
PATERNA

ITALY

VENETO
PADOVA

Molecular diagnosis of rare cataract [panel of genes]
Research&Innovation S.r.l. (R&I Genetics)

SPAIN

Madrid
MADRID

FRANCE

ILE-DE-FRANCE
PARIS

Biochemical diagnosis of chondrodysplasia punctata rhizomelic form
Faculté de Médecine Pierre et Marie Curie - Hôpital Saint-Antoine

ITALY

LIGURIA
GENOVA

Biochemical diagnosis of peroxisomal diseases (metabolite analysis)
IRCCS Istituto G. Gaslini - Ospedale Pediatrico

ITALY

LAZIO
ROMA

Biochemical diagnosis of chondrodysplasia punctata, rhizomelic form
IRCCS Ospedale Pediatrico Bambino Gesù - SEDE SAN PAOLO

PORTUGAL

NORTE
PORTO

Biochemical diagnosis of chondrodysplasia punctata rhizomelic form types 1, 2 and 3
CGMJM - Centro de Genética Médica Jacinto Magalhães

UNITED KINGDOM

Greater London
LONDON

Biochemical diagnosis of Peroxisomal disorders (Analyte: Very Long Chain Fatty Acids)
Great Ormond Street Hospital for Children, NHS Foundation Trust

ITALY

VENETO
PADOVA

Biochemical diagnosis of chondrodysplasia punctata, rhizomelic type
Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano

FRANCE

ILE-DE-FRANCE
PARIS

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of chondrodysplasia punctata, rhizomelic type (PEX7, GNPAT, AGPS genes)
LabGenetics - Laboratorio de Genética Clínica, S.L.

SPAIN

Castilla - León
SALAMANCA

GERMANY

Niedersachsen
GÖTTINGEN

GERMANY

Nordrhein-Westfalen
DÜSSELDORF

Array-CGH in case of unexplained developmental delay
Praenatal-Medizin und Genetik, Düsseldorf

FRANCE

GRAND-EST
VANDOEUVRE-LÈS-NANCY

Diagnosis of peroxisomal diseases (Panel)
CHU de Nancy - Hôpitaux de Brabois