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Funded by an IRDiRC member =

Research projects

GERMANY

Baden-Württemberg
ULM

GERMANY

Nordrhein-Westfalen
ESSEN

GERMANY

Nordrhein-Westfalen
ESSEN

SPAIN

País Vasco
VITORIA-GASTEIZ

Funded by an IRDiRC memberNew genetic mechanisms involved in imprinting disorders
HUA - Hospital Universitario Araba. Sede Txagorritxu
Laboratorio de Genética Molecular

SPAIN

País Vasco
VITORIA-GASTEIZ

Funded by an IRDiRC memberImprinting disorders: low grade mosaicism or new candidate genes? - ES
HUA - Hospital Universitario Araba. Sede Txagorritxu
Laboratorio de Genética Molecular

CANADA

Alberta
EDMONTON

Funded by an IRDiRC memberAutonomic nervous system function and metabolic profiling in children with PWS
University of Alberta
Department of Pediatrics, Division of Endocrinology and Metabolism

CANADA

Alberta
EDMONTON

Evidence-based approach to dietary management of Prader Willi Syndrome
University of Alberta
Department of Pediatrics, Division of Endocrinology and Metabolism

FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Funded by an IRDiRC memberPostnatal development of the brain oxytocin system and Prader-Willi syndrome
Parc scientifique et technologiques de Luminy
Institut de Neurobiologie de la Méditerranée

ITALY

LAZIO
PASSOSCURO

Prader-Willi syndrome: genetic, metabolic and endocrine functional neuroanatomy
Ospedale Pediatrico Bambino Gesù
U.O. di Endocrinologia

ITALY

LOMBARDIA
CUSANO MILANINO

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

PWS: Prader-Willi Syndrom: a model linking gene expression, obesity and mental health (coordination)
Developmental Psychiatry - University of Cambridge
Learning Disabilities Research Group

DENMARK

Nordjylland
AALBORG

SWITZERLAND

Suisse Alémanique
SCHLIEREN

Identification of novel autosomal genes causing mental retardation
Universität Zürich
Institut für Medizinische Genetik

UNITED KINGDOM

Lothian
EDINBURGH

Genetic disorders of human brain development
Western General Hospital
MRC Human Genetics Unit

UNITED KINGDOM

Cambridgeshire
HINXTON

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

UNITED KINGDOM

Devon
EXETER

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

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

Multicentric Research projects