Title of article
High Frequency of Loss of Heterozygosity for 1p35–p36 (D1S247) in Wilms Tumor
Author/Authors
Steinberg، نويسنده , , Ran and Freud، نويسنده , , Enrique and Zer، نويسنده , , Michael and Ziperman، نويسنده , , Izolda and Goshen، نويسنده , , Yacov and Ash، نويسنده , , Shifra and Stein، نويسنده , , Jeremiah and Zaizov، نويسنده , , Rina and Avigad، نويسنده , , Smadar، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2000
Pages
4
From page
136
To page
139
Abstract
We analyzed the loss of heterozygosity (LOH) for 1p in 18 Wilms tumors using a panel of 11 polymorphic markers. Loss of heterozygosity was identified in 56% of the tumors. The smallest region of overlap was defined for marker D1S247, underlying the 1p35–1p36.1 locus. This is the highest LOH frequency for 1p, or for the well-defined 11p13 and 11p15.5 loci. Based on the fact that tumors of all stages, with both favorable and unfavorable histology, exhibited LOH, we suggest that the 1p35–1p36.1 locus is involved in the etiology of Wilms tumor.
Journal title
Cancer Genetics and Cytogenetics
Serial Year
2000
Journal title
Cancer Genetics and Cytogenetics
Record number
1822607
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