The direct early diagnosis of cystic fibrosis by the detection of the deltaF508 CFTR gene mutation in a prematurely delivered boy-Reference-Cited by-同舟云学术

The direct early diagnosis of cystic fibrosis by the detection of the deltaF508 CFTR gene mutation in a prematurely delivered boy

Published:2008-06-28 Issue:3 Volume:39 Page:219-222
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Macek Milan,Macek Milan,Stuhrmann Manfred,Kulovany Eduard,Dolanská Marie,Koukolík František,Boehm Ingolf,Hronková Jana,Ježková Zdeňka,Paulová Magdalena,Martanová Hana,Zach Jiří,Reis André,Sperling Karl,Schmidtke Jörg

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1991.tb03015.x/fullpdf

Reference11 articles.

1. Linkage disequilibrium, cystic fibrosis and genetic counselling;Beaudet;Am. J. Hum. Genet.,1989

2. Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer;Drumm;Cell,1990

3. DeltaF508 gene deletion in cystic fibrosis in Southern Europe;Estivill;Lancet,1989

4. Prenatal diagnosis of cystic fibrosis by DNA amplification for the detection of KM19 polymorphism;Feldman;Lancet,1988

5. Identification of the cystic fibrosis gene: genetic analysis;Kerem;Science,1989

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