Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardation

✍ Scribed by Emily Chen; Elise Obolensky; Katherine A. Rauen; Lisa G. Shaffer; Xu Li

• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 255 KB
• Volume: 146A
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.32437