✦ LIBER ✦

The impact of cystic fibrosis on neonatal intestinal obstruction: the need for prenatal/neonatal screening

✍ Scribed by G. Casaccia; A. Trucchi; A. Nahom; L. Aite; V. Lucidi; C. Giorlandino; P. Bagolan

Book ID: 106054733
Publisher: Springer-Verlag
Year: 2003
Tongue: English
Weight: 161 KB
Volume: 19
Category: Article
ISSN: 0179-0358
DOI: 10.1007/s00383-002-0781-8

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Demographics of the UK cystic fibrosis p

Demographics of the UK cystic fibrosis population: implications for neonatal screening

✍ McCormick, Jonathan (author);Green, Michael W. (author);Mehta, Gita (author);Cul 📂 Article 📅 2002 🏛 Nature Publishing Group 🌐 English ⚖ 139 KB

Demographics of the UK cystic fibrosis p

Demographics of the UK cystic fibrosis population: implications for neonatal screening

✍ McCormick, Jonathan (author);Green, Michael W. (author);Mehta, Gita (author);Cul 📂 Article 📅 2002 🏛 Nature Publishing Group 🌐 English ⚖ 139 KB

Retrospective study of the cystic fibros

Retrospective study of the cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Guthrie cards from a large cohort of neonatal screening for cystic fibrosis

✍ C. Verlingue; B. Mercier; I. Lecoq; M. P. Audrézet; D. Laroche; G. Travert; C. F 📂 Article 📅 1994 🏛 Springer 🌐 English ⚖ 707 KB

The cystic fibrosis transmembrane conductance regulator (CFTR) gene encodes a cAMP-activated chloride channel, and in individuals with both alleles of the gene mutated, symptoms of CF disease are manifest. With more than 300 mutations so far described in the gene the profile of mutant alleles in a p