Prader–Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15—case report plus review of similar cases

✍ Scribed by Thomas Liehr; Elke Brude; Gabriele Gillessen-Kaesbach; Rainer König; Kristin Mrasek; Ferdinand von Eggeling; Heike Starke

• Book ID: 116432758
• Publisher: Elsevier Science
• Year: 2005
• Tongue: English
• Weight: 160 KB
• Volume: 48
• Category: Article
• ISSN: 1769-7212
• DOI: 10.1016/j.ejmg.2005.01.004