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Projetos de investigação
ALEMANHA
Sachsen-Anhalt
MAGDEBURG
EUROlinkCAT: Establishing a linked European Cohort of Children with Congenital Anomalies (partner DE)
Universitätsklinikum Magdeburg A.ö.R
MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
ALEMANHA
Niedersachsen
GÖTTINGEN
Elucidating the pathogenesis of Kabuki syndrome and a possible molecular genetic link between the two malformation syndromes CHARGE and Kabuki
Institut für Humangenetik der Universität Göttingen
Institut für Humangenetik
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Investigation of x chromosome haploinsufficiency on germ cell development using t
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Gender-specific effects in physiology; pathophyiology and longevity
Institution: Information not provided - US
FRANCA
ILE-DE-FRANCE
LE KREMLIN-BICÊTRE
Survey of the interest of ovarian cortex cryoconservation of girls affected by Turner syndrome: search for clinical and hormonal critera to select patients and caryotypic correlations
Hôpital Bicêtre, GHU APHP. Université Paris Saclay
Service d'Endocrinologie et Diabète de l'Enfant
JAPAO
JAPAN
TOKYO
Study aiming at elucidation of the pathoiogy of multiple congenital anomaly syndrome by utilizing diseases- specific iPSCs and development of novel treatment methods
Keio University School of Medicine
ALEMANHA
Nordrhein-Westfalen
BONN
Luto Study: Systematic Investigation of the Molecular Causes of Congenital Uro-Rectal Malformations for Subjects and Families with LUTO (Lower Urinary Tract Obstruction)
Universitätsklinikum Bonn (AöR)
Institut für Humangenetik
ALEMANHA
Nordrhein-Westfalen
BONN
Luto Study: Systematic Investigation of the Molecular Causes of Congenital Uro-Rectal Malformations for Subjects and Families with LUTO (Lower Urinary Tract Obstruction)
Universitätsklinikum Bonn (AöR)
Universitätsklinikum Bonn
ITALIA
CAMPANIA
NAPOLI
Analysis of ARX mutations in patients with neurodevelopmental diseases (NDDs)
Istituto di Genetica e Biofisica "Adriano Buzzati Traverso" - CNR
Human Molecular Neurogenetics Laboratoty
ALEMANHA
Baden-Württemberg
TÜBINGEN
ESPED-study: Omphaloceles and Associated Malformations in Preterm and Term Newborns
Universitätsklinik für Kinder- und Jugendmedizin Tübingen
Abteilung für Neonatologie
SUECIA
Region Stockholm
STOCKHOLM
Molecular and clinical studies of bladder exstrophy and congenital adrenal hyperplasia
Karolinska Institutet - Solna
Department of Women's and Children's Health
ALEMANHA
Baden-Württemberg
TÜBINGEN
Impact of MRKH syndrome in somatic, social and mental health
Universitäts-Frauenklinik Tübingen
Frauenklinik
ALEMANHA
Baden-Württemberg
TÜBINGEN
Investigation of histological and immunohistochemical organisation of the uterine rudiments in MRKH patients
Universitäts-Frauenklinik Tübingen
Frauenklinik
ALEMANHA
Baden-Württemberg
TÜBINGEN
Impact of MRKH syndrome in somatic, social and mental health
ViTa-Gebäude Talklinikum
Abteilung Psychosomatische Medizin und Psychotherapie am Universitätsklinikum Tübingen
Projetos de investigação multicêntricos
- Radboudumc - Radboud universitair medisch centrum
- Afdeling Kinderurologie
- Universitätsklinikum Magdeburg A.ö.R
- MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
- Universitätsklinikum Aachen
- Institut für Humangenetik
- Radboudumc - Radboud universitair medisch centrum
- Afdeling Genetica
- UCL Institute for Women's Health
- UCLH Women's Health Division
PAISES BAIXOS
Gelderland
NIJMEGEN
EUROSTEC: soft tissue engineering for congenital birth defects: New treatment modalities for spina bifida, urogenitial and abdominal wall defects (COMPLETED)
ALEMANHA
Sachsen-Anhalt
MAGDEBURG
International Clearinghouse for Birth Defects Monitoring Systems
ALEMANHA
Nordrhein-Westfalen
AACHEN
EUCID.net: European Congenital Imprinting Disorders Network
PAISES BAIXOS
Gelderland
NIJMEGEN
EURO-MRX: European mental retardation consortium
REINO UNIDO
Greater London
LONDON