Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib)

✍ Scribed by Murat Bastepe; Özge Altug-Teber; Chhavi Agarwal; Sharon E. Oberfield; Michael Bonin; Harald Jüppner

• Book ID: 116324086
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 432 KB
• Volume: 48
• Category: Article
• ISSN: 8756-3282
• DOI: 10.1016/j.bone.2010.10.168