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PRENATAL DIAGNOSIS IN CYSTIC FIBROSIS


Book ID
123252637
Publisher
The Lancet
Year
1985
Tongue
English
Weight
158 KB
Volume
325
Category
Article
ISSN
0140-6736

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๐Ÿ“œ SIMILAR VOLUMES


PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS IN
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

Use of linkage disequilibrium data in pr
โœ Lisa Strain; Ann Curtis; Moira Mennie; Susan Holloway; David J. H. Brock ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› Springer ๐ŸŒ English โš– 332 KB

Parents at risk of bearing a child with cystic fibrosis, and who have no living affected child, often use prenatal diagnosis based on microvillar enzyme assay in second-trimester amniotic fluid samples. If enzyme levels are abnormal and the pregnancy is terminated, it is possible in principle to use