A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5
- 1 February 1996
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 97 (2) , 163-170
- https://doi.org/10.1007/bf02265259
Abstract
No abstract availableKeywords
This publication has 52 references indexed in Scilit:
- Integrated human genome–wide maps constructed using the CEPH reference panelNature Genetics, 1994
- A microsatellite-based index map of human chromosome 11Human Molecular Genetics, 1993
- Deletion of WT1 and WIT1 Genes and Loss of Heterozygosity on Chromosome 11p in Wilms Tumors in JapanJapanese Journal of Cancer Research, 1993
- Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprintedHuman Molecular Genetics, 1993
- Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumorsGenomics, 1992
- Dinucleotide repeat polymorphisms at the D11S439 and HBB lociHuman Molecular Genetics, 1992
- Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumorGenomics, 1990
- 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
- Loss of genes on the short arm of chromosome 11 in bladder cancerNature, 1985