Prenatal diagnosis for cystic fibrosis using SSCP analysis-Reference-Cited by-同舟云学术

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Prenatal diagnosis for cystic fibrosis using SSCP analysis

Published:1993-02 Issue:2 Volume:13 Page:147-148
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Desgeorges Marie,Boulot Pierre,Kjellberg Paule,Lefort Geneviève,Rolland Michel,Demaille Jacques,Claustres Mireille

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference5 articles.

1. , , , (1992). Analysis of 30 known cystic fibrosis mutations account for 27% of non-ΔF508 chromosomes in southern France, Hum. Genet., in press.

2. Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients

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. Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

Cited by 2 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. Prenatal diagnosis of Crigler-Najjar syndrome type I by single-strand conformation polymorphism (SSCP);Prenatal Diagnosis;2002

2. PRENATAL DIAGNOSIS OF GLYCOGEN STORAGE DISEASE TYPE 1a BY SINGLE STRANDED CONFORMATION POLYMORPHISM (SSCP);Prenatal Diagnosis;1996-09

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