Autosomal dominant transmission of congenital hypothyroidism, neonatal respiratory distress, and ataxia caused by a mutation of NKX2-1

✍ Scribed by Daniel A. Doyle; Iris Gonzalez; Becky Thomas; Mena Scavina

• Book ID: 116682721
• Publisher: Elsevier Science
• Year: 2004
• Tongue: English
• Weight: 115 KB
• Volume: 145
• Category: Article
• ISSN: 1097-6833
• DOI: 10.1016/j.jpeds.2004.04.011