Detection of novel and rare mutations in exon 4 of the cystic fibrosis gene by SSCP
- PMID: 1284529
- DOI: 10.1093/hmg/1.6.439
Detection of novel and rare mutations in exon 4 of the cystic fibrosis gene by SSCP
Similar articles
-
G27X: a novel mutation in exon 2 of the CF gene.Hum Mol Genet. 1992 Sep;1(6):445. doi: 10.1093/hmg/1.6.445. Hum Mol Genet. 1992. PMID: 1284531 No abstract available.
-
Screening for CF mutations in adult cystic fibrosis patients with a directed and optimized SSCP strategy.Hum Mutat. 1994;3(3):231-8. doi: 10.1002/humu.1380030309. Hum Mutat. 1994. PMID: 7517265
-
High percentage acrylamide gels improve resolution in SSCP analysis.Nucleic Acids Res. 1992 Dec 25;20(24):6741-2. doi: 10.1093/nar/20.24.6741. Nucleic Acids Res. 1992. PMID: 1282707 Free PMC article.
-
Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a report from the Cystic Fibrosis Genetic Analysis Consortium.Hum Mutat. 1992;1(3):197-203. doi: 10.1002/humu.1380010304. Hum Mutat. 1992. PMID: 1284534 Review.
-
The spectrum of cystic fibrosis mutations.Trends Genet. 1992 Nov;8(11):392-8. doi: 10.1016/0168-9525(92)90301-j. Trends Genet. 1992. PMID: 1279852 Review.
Cited by
-
Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients.Hum Genet. 1994 Nov;94(5):533-42. doi: 10.1007/BF00211022. Hum Genet. 1994. PMID: 7525450
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases