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Funded by an IRDiRC member =

Research projects

GERMANY

Hamburg
HAMBURG

Genotype-phenotype correlation of patients with WT1 gene mutation
UKE - Universitätsklinikum Hamburg-Eppendorf
Klinik und Poliklinik für Kinder- und Jugendmedizin

FRANCE

ILE-DE-FRANCE
PARIS

Funded by an IRDiRC memberEURENOMICS: European Consortium for High-Throughput Research in Rare Kidney Diseases - FR
CHU Paris - Hôpital Necker-Enfants Malades
Laboratoire de Génétique Moléculaire

GERMANY

Baden-Württemberg
HEIDELBERG

Li-Fraumeni syndrome-cancer predisposition syndrome registry
Deutsches Krebsforschungszentrum
KITZ - Hopp-Kindertumorzentrum Heidelberg

GERMANY

Niedersachsen
HANNOVER

Li-Fraumeni syndrome-cancer predisposition syndrome registry
Medizinische Hochschule Hannover
Klinik für Pädiatrische Hämatologie und Onkologie

SPAIN

Cataluña
BARCELONA

Funded by an IRDiRC memberGenomic study of early-onset nephropathies
Fundació Puigvert
Laboratorio de Biología Molecular

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

Funded by an IRDiRC memberNIHR BioResource - Rare Disease: MPMT - Multiple primary malignant tumours
Addenbrooke's Hospital
Academic Department of Medical Genetics

BELGIUM

VLAAMS BRABANT
LEUVEN

Funded by an IRDiRC memberEURENOMICS: European Consortium for High-Throughput Research in Rare Kidney Diseases - BE
University Hospitals Leuven - Gasthuisberg
Pediatric Nephrology and Organ transplantation

FRANCE

ILE-DE-FRANCE
GENNEVILLIERS

Funded by an IRDiRC memberAnnouncement of a severe renal fetal pathology detected during pregnancy
Université de Cergy-Pontoise
Ecole, Mutations, Apprentissages

ITALY

CAMPANIA
NAPOLI

Funded by an IRDiRC memberTelethon Undiagnosed Disease Program - Revised Proposal
Azienda Ospedaliera Universitaria - Seconda Università degli Studi di Napoli
Laboratorio di Genetica Medica

ITALY

LOMBARDIA
RANICA

Funded by an IRDiRC memberEURENOMICS: European Consortium for High-Throughput Research in Rare Kidney Diseases - IT
Istituto di Ricerche Farmacologiche Mario Negri
Centro di Ricerche Cliniche per le Malattie Rare

NETHERLANDS

Gelderland
NIJMEGEN

EUNEFRON: rare disorders of the collecting dust (WP5)
Radboudumc - Radboud universitair medisch centrum
Afdeling Fysiologie

SWEDEN

Stockholms läns landsting
STOCKHOLM

Inborn errors of endocrinology and metabolism
Karolinska Institutet - Solna
Department of Molecular Medicine and Surgery

UNITED KINGDOM

Devon
EXETER

Exploring the Genetics of Renal Developmental Disease
Royal Devon and Exeter Hospital - Wonford site
Department of Urology

UNITED KINGDOM

Devon
EXETER

Funded by an IRDiRC memberThe role and regulation of Hepatocyte Nuclear Factor-1 Beta in man
Royal Devon and Exeter Hospital - Wonford site
Department of Urology

UNITED KINGDOM

Glasgow
GLASGOW

Funded by an IRDiRC memberThe International DSD Network (I-DSD)
University of Glasgow, Kelvin Building
College of Medical, Veterinary & Life Sciences

SWITZERLAND

Suisse Alémanique
BASEL

Massively parallel sequencing for gene discovery in lethal fetal disorders
Universitätsspital Basel
Abteilung für Medizinische Genetik

UNITED KINGDOM

Cambridgeshire
HINXTON

The Deciphering Developmental Disorders (the DDD study)
Wellcome Trust Sanger Institute
DECIPHER

Multicentric Research projects