Showing results (241-250 of 340) with videos related to
Sort By:
Pageof 34
Cancer Research|November 14, 1997
Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumorsP L Dahia, D J Marsh, Z Zheng, et al.The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|October 30, 2001
Reduced employment in caregivers of frail elders: impact of ethnicity, patient clinical characteristics, and caregiver characteristicsK E Covinsky, C Eng, L Y Lui, et al.Gastrointestinal Endoscopy|December 7, 2007
Complications after ERCP in patients with primary sclerosing cholangitisJason P Etzel, Sue C Eng, Cynthia W Ko, et al.Oncogene|January 23, 1997
Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regionsF Kerangueven, F Eisinger, T Noguchi, et al.Journal of the National Cancer Institute|July 21, 1993
Mortality from second tumors among long-term survivors of retinoblastomaC Eng, F P Li, D H Abramson, et al.Gut|April 17, 2001
Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung diseaseR Gath, A Goessling, K M Keller, et al.Molecular Cell|July 8, 1999
Loss-of-function mutations in PPAR gamma associated with human colon cancerP Sarraf, E Mueller, W M Smith, et al.Nature Genetics|January 1, 1994
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTCL M Mulligan, C Eng, C S Healey, et al.The Journal of Clinical Endocrinology and Metabolism|September 16, 1999
Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutationsE M Duerr, O Gimm, D S Neuberg, et al.Nature Genetics|November 1, 1996
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung diseaseR Salomon, T Attié, A Pelet, et al.Pageof 34