Maternal 21-hydroxylase deficiency and uniparental isodisomy of chromosome 6 and X results in a child with 21-hydroxylase deficiency and Klinefelter syndrome

✍ Scribed by Elizabeth A. Parker; Karine Hovanes; John Germak; Forbes Porter; Deborah P. Merke

• Publisher: John Wiley and Sons
• Year: 2006
• Tongue: English
• Weight: 129 KB
• Volume: 140A
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.31408