Molecular genetic analysis of recessive mutations at a heterozygous autosomal locus in human cells
- 1 March 1990
- journal article
- research article
- Published by Elsevier in Mutation Research
- Vol. 229 (1), 89-102
- https://doi.org/10.1016/0027-5107(90)90011-r
Abstract
No abstract availableKeywords
This publication has 51 references indexed in Scilit:
- DNA methylation and genetic inactivation at thymidine kinase locus: Two different mechanisms for silencing autosomal genesSomatic Cell and Molecular Genetics, 1988
- Molecular characterization of 15 rearrangements among 90 human in vivo somatic mutants shows that deletions predominate.Molecular and Cellular Biology, 1987
- Recessive mutant genes predisposing to human cancerMutation Research/Reviews in Genetic Toxicology, 1986
- Alterations of the hprt gene in human in vivo-derived 6-thioguanine-resistant T lymphocytesNature, 1985
- Human thymidine kinase gene: molecular cloning and nucleotide sequence of a cDNA expressible in mammalian cells.Molecular and Cellular Biology, 1984
- Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumoursNature, 1984
- Amplification versus mutation as a mechanism for reversion of anHGPRT mutationSomatic Cell and Molecular Genetics, 1984
- Expression of recessive alleles by chromosomal mechanisms in retinoblastomaNature, 1983
- Deletion and amplification of the HGPRT locus in Chinese hamster cells.Molecular and Cellular Biology, 1983
- High-frequency nonrandom mutational event at the adenine phosphoribosyltransferase (aprt) locus of sib-selected CHO variants heterozygous foraprtSomatic Cell and Molecular Genetics, 1982