Author:
Augarten A.,Yahav Y.,Szeinberg A.,Noiman S.,Gazit E.,Kerem B-S.,Rivlin Y.,Tal A.,Blau H.,Ben-Tur L.,Kerem E.
Reference10 articles.
1. Identification of the cystic fibrosis gene: genetic analysis;Kerem;Science,1989
2. The relation between genotype and phenotype in cystic fibrosis-analysis of the most common mutation (ΔF508);Kerem;N Engl J Med,1990
3. Linked marker haplotypes and the ΔF508 mutation in adults with mild pulmonary disease and cystic fibrosis;Santis;Lancet,1990
4. Association of nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease;Shoshani;Am J Hum Genet,1992
5. Identification of a homozygous point mutation in intron 19 in an inbred CF patient with mild disease and normal sweat chloride: creation of an alternative splice site resulting in base-sequence insertion in CFTR coding region between exon 19 and 20;Highsmith;Pediatr Pulmonol,1991
Cited by
124 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献