A Simple Assay for the Screening of the Cystic Fibrosis Allele in Carriers of the Phe508 Deletion Mutation
- 1 August 1990
- journal article
- research article
- Published by Elsevier in Mayo Clinic Proceedings
- Vol. 65 (8) , 1072-1076
- https://doi.org/10.1016/s0025-6196(12)62719-0
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Identification of the Cystic Fibrosis Gene: Chromosome Walking and JumpingScience, 1989
- Identification of the Cystic Fibrosis Gene: Genetic AnalysisScience, 1989
- Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNAScience, 1989
- Carrier Identification of Cystic Fibrosis by Recombinant DNA TechniquesMayo Clinic Proceedings, 1989
- PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS BY DNA AMPLIFICATION FOR DETECTION OF KM-19 POLYMORPHISMThe Lancet, 1988
- Experience with New DNA Markers for the Diagnosis of Cystic FibrosisNew England Journal of Medicine, 1988
- A candidate for the cystic fibrosis locus isolated by selection for methylation-free islandsNature, 1987
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985
- Localization of cystic fibrosis locus to human chromosome 7cen–q22Nature, 1985
- A closely linked genetic marker for cystic fibrosisNature, 1985