An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor
- 1 June 1990
- Vol. 61 (7) , 1257-1269
- https://doi.org/10.1016/0092-8674(90)90690-g
Abstract
No abstract availableKeywords
This publication has 61 references indexed in Scilit:
- Hypomethylation of ras oncogenes in primary human cancersPublished by Elsevier ,2005
- Oncogenic Point Mutations in the Human Retinoblastoma Gene: Their Application to Genetic CounselingNew England Journal of Medicine, 1989
- Mutations in the p53 gene occur in diverse human tumour typesNature, 1989
- A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndromeGenomics, 1989
- Chromosome 17 Deletions and p53 Gene Mutations in Colorectal CarcinomasScience, 1989
- Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13Nature, 1988
- Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11Nature, 1988
- Homozygous deletion of a DNA marker from chromosome 11p13 in sporadic Wilms tumorGenomics, 1988
- Homozygosity of Chromosome 13 in RetinoblastomaNew England Journal of Medicine, 1984
- Abnormality of chromosome 11 in patients withfeatures of Beckwith-Wiedemann syndromeThe Journal of Pediatrics, 1983