✦ LIBER ✦

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

✍ Scribed by Amselem, Serge; Netchine, Irène; Sobrier, Marie-Laure; Krude, Heiko; Schnabel, Dirk; Maghnie, Mohamed; Marcos, Elisabeth; Duriez, Bénédicte; Cacheux, Valère; Moers, Arpard v.; Goossens, Michel; Grüters, Annette

Book ID: 109828268
Publisher: Nature Publishing Group
Year: 2000
Tongue: English
Weight: 611 KB
Volume: 25
Category: Article
ISSN: 1061-4036
DOI: 10.1038/76041

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutations within the transcription facto

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD)

✍ James P. G. Turton; Ameeta Mehta; Jamal Raza; Kathryn S. Woods; Anatoly Tiulpako 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 242 KB

Adrenocorticotrope Deficiency with Clini

Adrenocorticotrope Deficiency with Clinical Evidence for Late Onset in Combined Pituitary Hormone Deficiency Caused by a Homozygous 301–302delAG Mutation of the PROP1 Gene

✍ C. Lamesch; S. Neumann; R. Pfäffle; W. Kiess; R. Paschke 📂 Article 📅 2002 🏛 Springer US 🌐 English ⚖ 253 KB

Mutation analysis of POUF-1, PROP-1 and

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

✍ L. A. Rainbow; S. A. Rees; M. G. Shaikh; N. J. Shaw; T. Cole; T. G. Barrett; J. 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 137 KB