Clinical utility gene card for: Prader-Willi Syndrome

Affiliations

¹ Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
² Department of Pediatrics, Division of Medical Genetics, University of California, San Francisco, CA, USA.
³ Division of Genetics and Metabolism, Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL, USA.
⁴ Institut für Humangenetik, Universität zu Lübeck, Lübeck, Germany.
⁵ 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.

Karin Buiting et al. Eur J Hum Genet. 2014 Sep.

. 2014 Sep;22(9).

doi: 10.1038/ejhg.2014.66. Epub 2014 Apr 16.

¹ Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
² Department of Pediatrics, Division of Medical Genetics, University of California, San Francisco, CA, USA.
³ Division of Genetics and Metabolism, Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL, USA.
⁴ Institut für Humangenetik, Universität zu Lübeck, Lübeck, Germany.
⁵ 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.

No abstract available

References

1. Cassidy SB, Schwartz S, Miller JL, Driscoll DJ. Prader-Willi syndrome. Genet Med. 2012;14:10–26. - PubMed
1. Ramsden SC, Clayton-Smith J, Birch R, Buiting K. Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes. BMC Med Genet. 2010;11:11–70. - PMC - PubMed
1. Buiting K. Prader-Willi syndrome and Angelman syndrome. Am J Med Genet Part C. 2010;154C:365–376. - PubMed