Use of the chemical cleavage of mismatch method for prenatal deficiency diagnosis of alpha-1-antitrypsin-Reference-Cited by-同舟云学术

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Use of the chemical cleavage of mismatch method for prenatal deficiency diagnosis of alpha-1-antitrypsin

Published:1992-02 Issue:2 Volume:12 Page:133-137
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Forrest S. M.,Dry P. J.,Cotton R. C. H.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference10 articles.

1. PRENATAL DIAGNOSIS OF ALPHA-1-ANTITRYPSIN DEFICIENCY USING POLYMERASE CHAIN REACTION

2. Improvement of PCR amplified DNA sequencing with the aid of detergents

3. Detection of alpha1-antitrypsin genotypes by analysis of amplified DNA sequences

4. Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations.

5. , , , , (1991). Simultaneous screening for β-thalassemia mutations by chemical cleavage of mismatch, Genomics, in press.

Cited by 4 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. American Thoracic Society/European Respiratory Society Statement;American Journal of Respiratory and Critical Care Medicine;2003-10

2. Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII.;Proceedings of the National Academy of Sciences;1995-01-03

3. The use of chemical reagents in the detection of DNA mutations;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;1993-07

4. Single gene disorders affecting the gastrointestinal tract.;Gut;1993-04-01

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