Screening for cystic fibrosis gene mutations by multiplex DNA amplification
- 1 March 1992
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 88 (5) , 552-556
- https://doi.org/10.1007/bf00219343
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- The search for South European cystic fibrosis mutations: Identification of two new mutations, four variants, and intronic sequencesGenomics, 1991
- Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT)1Genomics, 1991
- CorrectionNew England Journal of Medicine, 1990
- A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator proteinNature, 1990
- Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan familiesGenomics, 1990
- Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patientsCell, 1990
- Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplificationHuman Genetics, 1990
- Identification of the Cystic Fibrosis Gene: Genetic AnalysisScience, 1989
- Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplificationNucleic Acids Research, 1988
- Silver stain for detecting 10-femtogram quantities of protein after polyacrylamide gel electrophoresisAnalytical Biochemistry, 1983