๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Cystic fibrosis: Cell culture classes in a Danish population

โœ Scribed by B. Shannon Danes; B. Beck; E. Winge Flensborg

Book ID
119838625
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
378 KB
Volume
13
Category
Article
ISSN
0009-9163

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

The major cystic fibrosis mutation in a
The major cystic fibrosis mutation in a British population
โœ C. J. McMahon; S. A. Genet; H. R. Middleton-Price; P. Rutland; M. E. Pembrey; S. ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Springer ๐ŸŒ English โš– 152 KB

We have studied 72 families with at least one child with cystic fibrosis (CF); they were referred because they had requested pre-natal diagnosis in a future pregnancy. The AF508 mutation was found in 108/140 CF chromosomes (77%). In 41/72 families (57%), both parents carried a deleted chromosome and

PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS IN
PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS IN A HIGHLY HETEROGENEOUS POPULATION
โœ TERESA CASALS; JAVIER GIMENEZ; MARIA D. RAMOS; VIRGINIA NUNES; XAVIER ESTIVILL ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 974 KB

Cystic fibrosis (CF) is the most common autosomal recessive disease in Caucasian populations. The Spanish CF population is highly heterogeneous, with more than 70 different mutations causing CF. Since the CFTR gene was cloned, we have performed 81 prenatal diagnoses for 74 couples. Sixty-nine cases