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Projets de recherche
ALLEMAGNE
Thüringen
JENA
Collection and characterisation of cases with a small supernumerary marker chomosome with the goal of a genotype phenotype correlation
Institut für Humangenetik am Universitätsklinikum Jena
Institut für Humangenetik
ESPAGNE
Cataluña
BARCELONA
Early preganncy loss: genetic causes and recurrence risk
Hospital Clínic de Barcelona
Instituto Clínic de Ginecología, Obstetricia y Neonatología
FRANCE
BOURGOGNE-FRANCHE-COMTE
DIJON
Diagnostic des réarrangements chromosomiques et des mutations par séquençage haut-débit
CHU de Dijon - Plateau technique de Biologie
Laboratoire de génétique chromosomique et moléculaire
SUEDE
Stockholms läns landsting
STOCKHOLM
Chromosomal anomaly
Karolinska Universitetsjukhuset - Klinisk Genetik
Clinical Genetics (Klinisk genetik)
ALLEMAGNE
Baden-Württemberg
HEIDELBERG
Li-Fraumeni syndrome-cancer predisposition syndrome registry
Deutsches Krebsforschungszentrum
KITZ - Hopp-Kindertumorzentrum Heidelberg
ALLEMAGNE
Niedersachsen
HANNOVER
Li-Fraumeni syndrome-cancer predisposition syndrome registry
Medizinische Hochschule Hannover
Klinik für Pädiatrische Hämatologie und Onkologie
ITALIE
CAMPANIA
NAPOLI
Telethon Undiagnosed Disease Program - Revised Proposal
Azienda Ospedaliera Universitaria - Seconda Università degli Studi di Napoli
Laboratorio di Genetica Medica
ROYAUME-UNI
Cambridgeshire
CAMBRIDGE
NIHR BioResource - Rare Disease: MPMT - Multiple primary malignant tumours
Addenbrooke's Hospital
Academic Department of Medical Genetics
ROYAUME-UNI
Cambridgeshire
HINXTON
The Deciphering Developmental Disorders (the DDD study)
Wellcome Trust Sanger Institute
DECIPHER
ROYAUME-UNI
Devon
EXETER
Exploring the Genetics of Renal Developmental Disease
Royal Devon and Exeter Hospital - Wonford site
Department of Urology
Projets de recherche multicentriques
- Universitätsklinikum Magdeburg A.ö.R
- MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
- University of British Columbia
- Maternal Infant Child and Youth Research Network
- IRCCS Ospedale Pediatrico Bambino Gesù - SEDE GIANICOLO
- Servizio Clinico di Consulenza Genetica
- Institut Curie
- Macromolécules et Microsystèmes en Biologie et en Medecine
ALLEMAGNE
Sachsen-Anhalt
MAGDEBURG
International Clearinghouse for Birth Defects Monitoring Systems
CANADA
Colombie-Britannique
VANCOUVER
Maternal Infant Child and Youth Research Network (MICYRN)
ITALIE
LAZIO
ROMA
UnRareNet: a muticenter collaborative research network for the identification and study of rare undiagnosed patients (completed)
FRANCE
ILE-DE-FRANCE
ORSAY