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Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome
Rebecca L. Hood, Matthew A. Lines, Sarah M. Nikkel, Jeremy Schwartzentruber, Chandree Beaulieu, Małgorzata J.M. Nowaczyk, Judith Allanson, Chong Ae Kim, Dagmar Wieczorek, Jukka S. Moilanen, Didier Lacombe, Gabriele Gillessen-Kaesbach, Margo L. Whiteford, Caio Robledo D.C. Quaio, Israel Gomy, Debora R. Bertola, Beate Albrecht, Konrad Platzer, George McGillivray, Ruobing Zou
*Korrespondierende/r Autor/-in für diese Arbeit
- University of Windsor
- University of Ottawa
- Ottawa Hospital Research Institute
- McGill University
- Hamilton Health Sciences
- Unidade de Genética
- University of Sao Paulo
- Institut fur Humangenetik
- Universität Duisburg-Essen
- University of Oulu
- Service de Génétique Médicale
- Centre Hospitalier Universitaire (CHU) de Bordeaux
- Ferguson-Smith Centre for Clinical Gentetics
- Yorkhill Hospitals
- Royal Children's Hospital
- Department of Medical Genetics
- University of Calgary
- Department of Paediatrics and Child Health
- University of Manitoba
- Department of Biochemistry and Medical Genetics
- Department of Paediatrics
- University of Melbourne
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