✦ LIBER ✦

Molecular analysis of the PAX8 gene in a sample of Mexican patients with primary congenital hypothyroidism: identification of the recurrent p.Arg31His mutation

✍ Scribed by Miguel Angel Alcántara-Ortigoza; Ariadna González-del Angel; Víctor Martínez-Cruz; Marcela Vela-Amieva; Carmen Sánchez-Pérez; Rosario Moreno-Rojas; Bernardette Estandía-Ortega; Nancy Hernández-Martínez

Book ID: 108705014
Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 49 KB
Volume: 76
Category: Article
ISSN: 0300-0664
DOI: 10.1111/j.1365-2265.2011.04153.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Genetic analysis of the PAX8 gene in chi

Genetic analysis of the PAX8 gene in children with congenital hypothyroidism and dysgenetic or eutopic thyroid glands: identification of a novel sequence variant

✍ Massimo Tonacchera; Maria Elena Banco; Lucia Montanelli; Caterina Di Cosmo; Patr 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 254 KB

Mutation analysis of the NSD1 gene in a

Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth

✍ M. Cecconi; F. Forzano; D. Milani; S. Cavani; C. Baldo; A. Selicorni; C. Pantale 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 187 KB 👁 2 views

Molecular analysis of the fibrinogen gen

Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in theFGAandFGGgenes

✍ M. Neerman-Arbez; P. de Moerloose; A. Honsberger; G. Parlier; B. Arnuti; C. Biro 📂 Article 📅 2001 🏛 Springer 🌐 English ⚖ 56 KB