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Financiado por um membro do IRDiRC =

Projetos de investigação

ALEMANHA

Niedersachsen
GÖTTINGEN

Financiado por um membro do IRDiRCEUROMICRO: Primary monogenic microcephalies: from genetics to pathophysiology and the clinic (partner no 3) - DE
Institut für Humangenetik der Universität Göttingen
Institut für Humangenetik

CANADA

Ontario
OTTAWA, ONTARIO

Financiado por um membro do IRDiRCDetection and simulation of femoroacetabular impingement
University of Ottawa
School of Electrical Engineering and Computer Science (EECS)

DINAMARCA

Nordjylland
AALBORG

ESPANHA

Comunidad Valenciana
VALENCIA

ESPANHA

Madrid
MADRID

Financiado por um membro do IRDiRCWhole exome sequencing for the study of 30 children with developmental delay or moderate to severe
INGEMM - Instituto de Genética Médica y Molecular (IdiPAZ)
Sección de Genómica Estructural y Funcional

FRANCA

GRAND-EST
ILLKIRCH-GRAFFENSTADEN

Financiado por um membro do IRDiRCGenCognition: Genetic basis of intellectual disability and other cognitive disorders
Institut de génétique et de biologie moléculaire et cellulaire - IGBMC
Département Médecine translationnelle et neurogénétique

FRANCA

ILE-DE-FRANCE
PARIS

Financiado por um membro do IRDiRCStudy of a mouse model of Meier-Gorlin Syndrome based on a mutation in the conserved BAH domain of ORC1
Institut Cochin (INSERM U 1016 - CNRS UMR 8104 - Paris Descartes UMR-S1016)
Equipe "Epigénétique, Réplication de l'ADN et Cancer"

FRANCA

ILE-DE-FRANCE
PARIS

Financiado por um membro do 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

FRANCA

PAYS DE LA LOIRE
ANGERS

FRANCA

PAYS DE LA LOIRE
NANTES

In vivo modeling for the genetic diagnosis of intellectual disabilities
CHU de Nantes - Institut de Biologie
Laboratoire de génétique moléculaire

FRANCA

PAYS DE LA LOIRE
NANTES

Financiado por um membro do 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

ITALIA

CAMPANIA
NAPOLI

Financiado por um membro do IRDiRCTelethon Undiagnosed Disease Program - Revised Proposal
Azienda Ospedaliera Universitaria - Seconda Università degli Studi di Napoli
Laboratorio di Genetica Medica

REINO UNIDO

Cambridgeshire
HINXTON

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

REINO UNIDO

Devon
EXETER

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

REINO UNIDO

Lothian
EDINBURGH

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

REINO UNIDO

Tyne & Wear
NEWCASTLE UPON TYNE

ESDN: European Skeletal Dysplasia Network (coordination)
Newcastle upon Tyne Hospitals NHS Trust
Institute of Genetic Medicine

SUICA

Suisse Alémanique
BASEL

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

SUICA

Suisse Alémanique
SCHLIEREN

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

TURQUIA

TURKEY
ANKARA

CRANIRARE: an integrated clinical and scientific approach for craniofacial malformations (partner No. 5) - TR
Hacettepe University Faculty of Medicine
Chemical Engineering and Bioengineering Departments

TURQUIA

TURKEY
ANKARA

TURQUIA

TURKEY
ISTANBUL

Projetos de investigação multicêntricos