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Clinical utility gene card for: Prader-Willi Syndrome.
Buiting, Karin; Cassidy, Suzanne B; Driscoll, Daniel J; Gillessen-Kaesbach, Gabriele; Kanber, Deniz; Tauber, Maithé; Schwinger, Eberhard; Horsthemke, Bernhard.
Afiliação
  • Buiting K; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
  • Cassidy SB; Department of Pediatrics, Division of Medical Genetics, University of California, San Francisco, CA, USA.
  • Driscoll DJ; Division of Genetics and Metabolism, Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL, USA.
  • Gillessen-Kaesbach G; Institut für Humangenetik, Universität zu Lübeck, Lübeck, Germany.
  • Kanber D; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
  • Tauber M; 1] Centre de référence du syndrome de Prader-Willi, service d'endocrinologie, Hôpital des Enfants, CHU Toulouse, Toulouse, France [2] Centre de Physiopathologie de Toulouse Purpan, INSERM UMR 1043, Toulouse, France.
  • Schwinger E; Institut für Humangenetik, Universität zu Lübeck, Lübeck, Germany.
  • Horsthemke B; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Eur J Hum Genet ; 22(9)2014 Sep.
Article em En | MEDLINE | ID: mdl-24736734
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Testes Genéticos Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Testes Genéticos Idioma: En Ano de publicação: 2014 Tipo de documento: Article