Cystic fibrosis mutations delta F508 and G542X in Jewish patients.-Reference-Cited by-同舟云学术

Cystic fibrosis mutations delta F508 and G542X in Jewish patients.

Published:1992-02-01 Issue:2 Volume:29 Page:131-133
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Lerer I,Sagi M,Cutting G R,Abeliovich D

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference15 articles.

1. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA;Riordan, JR, Rommens; JM, Kerem; B.S.;Science,1989

2. Identification of the cystic fibrosis gene: genetic analysis;Kerem, B.S.; Rommens, J.M.; Buchanan, J.A.;Science,1989

3. Identification of mutations in the regions corresponding to two putative nucleotide (ATP)-binding folds of the;Kerem, B.S.; Zielenski, J.; Markiewicz, D.,1990

4. A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the CFTR protein;Cutting, G.R.; Kasch, L.M.; Rosenstein, B.J.;Nature,1990

5. Prenatal diagnosis of cystic fibrosis by DNA amplification for detection of KM-19 polymorphism;Feldman, G.L.; Williamson, R.; Beaudet, A.L.; O'Brien, W.E.;Lancet,1988

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