Loss of Heterozygosity at Polymorphic Chromosomal Loci in Patients with Malignant Melanoma.
- 1 May 1989
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 92 (s5) , 280S-283S
- https://doi.org/10.1111/1523-1747.ep13076687
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Human cancer and cellular oncogenesBiochemical Journal, 1987
- Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.Proceedings of the National Academy of Sciences, 1986
- Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition.Proceedings of the National Academy of Sciences, 1985
- Genetic Origin of Mutations Predisposing to RetinoblastomaScience, 1985
- Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumoursNature, 1984
- Loss of a Harvey ras allele in sporadic Wilms' tumourNature, 1984
- Development of homozygosity for chromosome 11p markers in Wilms' tumourNature, 1984
- Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumourNature, 1984
- Homozygosity of Chromosome 13 in RetinoblastomaNew England Journal of Medicine, 1984
- Expression of recessive alleles by chromosomal mechanisms in retinoblastomaNature, 1983