Risks of fetal cystic fibrosis based on linkage disequilibrium data
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00274147.pdf
Reference13 articles.
1. Beaudet A, Spence JE, O'Brien WE, Estivill X, Farrall M, Williamson R (1988) Experience with new DNA markers for the diagnosis of cystic fibrosis. N Engl J Med 318:50?51
2. Human genetics,1987
3. Brock DJH, Clarke HAK, Barron L (1988) Prenatal diagnosis of cystic fibrosis by microvillar enzyme assay on a sequence of 258 pregnancies. Hum Genet 78:271?275
4. Curtis A, Strain L, Mennie M, Holloway S, Raeburn JA, Besley GTN, Brock DJH (1988) First trimester prenatal diagnosis of cystic fibrosis using fibroblasts from a deceased index child to establish haplotypes. Prenat Diagn 8:625?628
5. Estivill X, Farrall M, Scambler PJ, Bell GM, Hawley KMF, Lench NJ, Bates GP, Kruyer HC, Frederick PA, Stanier P, Watson EK, Williamson R, Wainwright BJ (1987) A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands. Nature 326:840?845
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1. Prenatal prediction of cystic fibrosis in a mother homozygous for the ΔF508 mutation;Clinical Genetics;2008-06-28
2. Five years' experience of prenatal diagnosis of cystic fibrosis in the former U.S.S.R.;Prenatal Diagnosis;1992-07
3. Biochemical and Molecular Genetics of Cystic Fibrosis;Advances in Human Genetics;1991
4. Gradient of distribution in Europe of the major CF mutation and of its associated haplotype;Human Genetics;1990-09
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