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Mutations of the Cystic Fibrosis Gene and Intermediate Sweat Chloride Levels in Children

✍ Scribed by LEBECQUE, PATRICK; LEAL, TERESINHA; DE BOECK, CHRISTIANE; JASPERS, MARTINE; CUPPENS, HARRY; CASSIMAN, JEAN-JACQUES


Book ID
124077938
Publisher
American Thoracic Society
Year
2002
Tongue
English
Weight
80 KB
Volume
165
Category
Article
ISSN
1073-449X

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Sweat electrolyte and cystic fibrosis mu
✍ Rabbi-Bortolini, Eliete; Bernardino, Andr�a L.F.; Lopes, Adoris L.; Ferri, Adria 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 24 KB 👁 2 views

A total of 540 individuals with clinical signs suggestive of cystic fibrosis (CF) was studied. The sweat chloride was measured and the DF508, G542X, R553X, and W1282X mutations of the CF gene were screened by polymerase chain reaction (PCR). With this approach the diagnosis of CF was confirmed in 12