Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probes
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1989.tb02911.x/fullpdf
Reference22 articles.
1. Familial occurrence of meconium ileus;Allan;Eur. J. Pediatr.,1981
2. La maladie fibrokystique des parenchymes glandulaires, étude génétique de 41 familles;Bernheim;Pediatrie,1961
3. Prenatal diagnosis in 200 pregnancies with a l-in-4 risk of cystic fibrosis;Boué;Hum. Genet.,1986
4. A comparative study of microvillar enzyme activities in the prenatal diagnosis of cystic fibrosis;Brock;Prenat. Diagn.,1985
5. The incidence and genetics of cystic fibrosis;Brunecky;J. Med. Genet.,1972
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3. Correlation of phenotypic and genetic heterogeneity in cystic fibrosis: Variability in sweat electrolyte levels contributes to heterogeneity and is increased with the XV-2c/KM19 B haplotype;American Journal of Medical Genetics;1991-05-01
4. Consequences of prenatal diagnosis of cystic fibrosis on the reproductive attitudes of parents of affected children;Prenatal Diagnosis;1991-04
5. Gradient of distribution in Europe of the major CF mutation and of its associated haplotype;Human Genetics;1990-09
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