A Simple Assay for the Screening of the Cystic Fibrosis Allele in Carriers of the Phe508 Deletion Mutation-Reference-Cited by-同舟云学术

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A Simple Assay for the Screening of the Cystic Fibrosis Allele in Carriers of the Phe508 Deletion Mutation

Published:1990-08 Issue:8 Volume:65 Page:1072-1076
ISSN:0025-6196
Container-title:Mayo Clinic Proceedings
language:en
Short-container-title:Mayo Clinic Proceedings

Author:

CHONG GEORGE L.,THIBODEAU STEPHEN N.

Publisher

Elsevier BV

Subject

General Medicine

Reference26 articles.

1. Cystic fibrosis;Boat,1989

2. Carrier identification of cystic fibrosis by recombinant DNA techniques;Dawson;Mayo Clin Proc,1989

3. A closely linked genetic marker for cystic fibrosis;White;Nature,1985

4. Localization of cystic fibrosis locus to human chromosome 7cen-q22;Wainwright;Nature,1985

5. Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study;Beaudet;Am J Hum Genet,1986

Cited by 3 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

1. Cystic Fibrosis—Mutation Detection by Microarrays;Encyclopedia of Medical Genomics and Proteomics;2004-12

2. Molecular temporal bone pathology: III. Genotyping of the ΔF508 deletion in the DNA of patients with cystic fibrosis;The Laryngoscope;1998-08

3. Heteroduplex detection: Application to rapid prenatal diagnosis for a type of β-thalassaemia most commonly found in South China;Prenatal Diagnosis;1993-11

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