High Frequency of Loss of Heterozygosity for 1p35–p36 (D1S247) in Wilms Tumor
- 1 March 2000
- journal article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 117 (2) , 136-139
- https://doi.org/10.1016/s0165-4608(99)00165-x
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Germline and somatic abnormalities of chromosome 7 in Wilms' tumorCancer Genetics and Cytogenetics, 1994
- WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele originHuman Genetics, 1994
- Infrequent mutation of theWT1 gene in 77 Wilms' tumorsHuman Mutation, 1994
- Loss of heterozygosity at 11p13 in Wilms' tumours does not necessarily involve mutations in the WT1 geneBritish Journal of Cancer, 1993
- Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashionHuman Molecular Genetics, 1993
- Alternative splicing and genomic structure of the Wilms tumor gene WT1.Proceedings of the National Academy of Sciences, 1991
- Wilms Tumor Locus on 11p13 Defined by Multiple CpG Island-Associated TranscriptsScience, 1990
- Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumpingNature, 1990
- Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locusCell, 1990
- Association of Wilms's Tumor with Aniridia, Hemihypertrophy and Other Congenital MalformationsNew England Journal of Medicine, 1964