Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia

✍ Scribed by L. A. Rainbow; S. A. Rees; M. G. Shaikh; N. J. Shaw; T. Cole; T. G. Barrett; J. M. W. Kirk

• Book ID: 108703088
• Publisher: John Wiley and Sons
• Year: 2005
• Tongue: English
• Weight: 137 KB
• Volume: 62
• Category: Article
• ISSN: 0300-0664
• DOI: 10.1111/j.1365-2265.2004.02189.x