Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus
- 31 May 1991
- Vol. 10 (1) , 293-297
- https://doi.org/10.1016/0888-7543(91)90516-h
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor geneCell, 1990
- Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locusCell, 1990
- Definition of the limits of the Wilms tumor locus on human chromosome 11p13Genomics, 1990
- Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11Cell, 1988
- 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
- Identification of Germline and Somatic Mutations Affecting the Retinoblastoma GeneScience, 1988
- Homozygous deletion of a DNA marker from chromosome 11p13 in sporadic Wilms tumorGenomics, 1988
- A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcomaNature, 1986
- Retinoblastoma: Clues to Human OncogenesisScience, 1984