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Journal of the National Cancer Institute|April 1, 1982
Carotid body tumors in humans: genetics and epidemiologyD M Parry, F P Li, L C Strong, et al.Journal of the National Cancer Institute|February 5, 1992
RNA expression of the WT1 gene in Wilms' tumors in relation to histologyH Miwa, G E Tomlinson, C F Timmons, et al.Genomics|May 1, 1991
Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locusC C Ton, V Huff, K M Call, et al.Oncogene|December 1, 1993
The retinoblastoma-related gene, RB2, maps to human chromosome 16q12 and rat chromosome 19R S Yeung, D W Bell, J R Testa, et al.Oncogene|August 26, 1998
Telomerase activity during spontaneous immortalization of Li-Fraumeni syndrome skin fibroblastsL S Gollahon, E Kraus, T A Wu, et al.Human Genetics|August 14, 1998
Exclusion of a p53 germline mutation in a classic Li-Fraumeni syndrome familyS C Evans, B Mims, K M McMasters, et al.Oncogene|February 1, 1991
Tumorigenic transformation of spontaneously immortalized fibroblasts from patients with a familial cancer syndromeF Z Bischoff, L C Strong, S O Yim, et al.Cancer Research|April 16, 1998
Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumorsJ M McDonald, E C Douglass, R Fisher, et al.American Journal of Human Genetics|January 1, 1997
Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignanciesJ T Hecht, D Hogue, Y Wang, et al.American Journal of Human Genetics|May 1, 1987
Nonrandom loss of maternal chromosome 11 alleles in Wilms tumorsW T Schroeder, L Y Chao, D D Dao, et al.Pageof 13