Development of RNA-SSCP protocols for the identification and screening of CFTR mutations: Identification of two new mutations
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference14 articles.
1. Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations.
2. The search for South European cystic fibrosis mutations: Identification of two new mutations, four variants, and intronic sequences
3. Identification of the Cystic Fibrosis Gene: Genetic Analysis
4. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
5. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
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