Orphanet: Ricerca per malattia/gene
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Progetti di ricerca

SPAGNA

Madrid
MADRID

Finanziato da un ente associato a IRDiRCEvaluation of the use of the fetal exome as a tool for identifying the genetic basis of major ultrasound abnormalities
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en genética y herencia

BELGIO

ANTWERPEN
ANTWERPEN-EDEGEM

SEC: Sensitivity and Accuracy of Prenatal Diagnosis of Severe Congenital Heart Diseases in the Antwerp Region
University Hospital of Antwerp - UZA
Dienst gynaecologie-verloskunde, Prenatale diagnose

CANADA

Ontario
TORONTO

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCSTaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196

FRANCIA

PAYS DE LA LOIRE
NANTES

Finanziato da un ente associato a IRDiRCFROGH : FRench Regional Origins in Genetics for Health - FR
Institut de Recherche en Santé - Université de Nantes
L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291

GERMANIA

Berlin
BERLIN

EURIPIDES: European Registry for ICD and CRT devices in pediatrics and adults with congenital heart disease
Kompetenznetz Angeborene Herzfehler
Nationales Register für angeborene Herzfehler e. V.

GIAPPONE

JAPAN
TOKYO

Finanziato da un ente associato a IRDiRCFormation of integrated omics analysis base of refractory diseases in children and perinatal period
National Center for Child Health and Development
Research Institute

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCA powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US

BELGIO

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUXELLES

Treat vascular anomalies
de Duve Institute
Laboratory of Human Genetics

Progetti di ricerca multicentrici