Prenatal prediction of cystic fibrosis in a mother homozygous for the ΔF508 mutation
暂无分享,去创建一个
[1] H. Cuppens. Gradient of distribution in Europe of the major CF mutation and of its associated haplotype , 2006, Human Genetics.
[2] D. Brock,et al. Risks of fetal cystic fibrosis based on linkage disequilibrium data , 1989, Human Genetics.
[3] B. Strandvik,et al. Frequency of four cystic fibrosis mutations in a Swedish population , 1993, Acta paediatrica.
[4] M. Starborg,et al. Characterization of the frequency of delta F508 mutation and CF haplotypes in Swedish families , 1991, Clinical genetics.
[5] A. Read,et al. Testing for cystic fibrosis using allelic association. , 1989, Journal of medical genetics.
[6] A. Kitzis,et al. Usefulness of linkage disequilibrium of KM‐19 and XV‐2c DNA probes for genetic counselling in a high‐risk cf family , 1989, Prenatal diagnosis.
[7] A. Beaudet,et al. Linkage disequilibrium, cystic fibrosis, and genetic counseling. , 1989, American journal of human genetics.
[8] L. Tsui,et al. Identification of the cystic fibrosis gene: genetic analysis. , 1989, Science.
[9] X. Estivill,et al. A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands , 1987, Nature.
[10] H. Kollberg. INCIDENCE AND SURVIVAL CURVES OF CYSTIC FIBROSIS IN SWEDEN , 1982, Acta paediatrica Scandinavica.