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Gynecologic Oncology|November 21, 2007
Clustering of Lynch syndrome malignancies with no evidence for a role of DNA mismatch repairAshley S Case, Israel Zighelboim, David G Mutch, et al.Human Mutation|March 25, 1999
Germline mutations in the multiple endocrine neoplasia type 1 gene: evidence for frequent splicing defectsM G Mutch, W G Dilley, F Sanjurjo, et al.Proceedings of the National Academy of Sciences of the United States of America|February 15, 1994
Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2BK M Carlson, S Dou, D Chi, et al.Genome Medicine|May 6, 2015
Novel APC promoter and exon 1B deletion and allelic silencing in three mutation-negative classic familial adenomatous polyposis familiesYiing Lin, Shin Lin, Melanie D Baxter, et al.Henry Ford Hospital Medical Journal|January 1, 1992
Screening for multiple endocrine neoplasia type 2A with DNA-polymorphism analysisE M Lamothe, S A Narod, S Miller, et al.Journal of Molecular Biology|April 2, 2008
Regulation of RNA polymerase III transcription by Maf1 in mammalian cellsSarah J Goodfellow, Emma L Graham, Theodoros Kantidakis, et al.Gynecologic Oncology|November 26, 2015
The role of racial genetic admixture with endometrial cancer outcomes: An NRG Oncology/Gynecologic Oncology Group studyRodney P Rocconi, Heather A Lankes, William E Brady, et al.Gastroenterology|September 1, 1997
Prognostic value of chromosome 1p allelic loss in colon cancerO A Ogunbiyi, P J Goodfellow, G Gagliardi, et al.Plos One|May 1, 2013
CMS: a web-based system for visualization and analysis of genome-wide methylation data of human cancersFei Gu, Mark S Doderer, Yi-Wen Huang, et al.The Journal of Clinical Endocrinology and Metabolism|May 3, 2003
Endothelial function and coagulant factors in growth hormone-treated hypopituitary adults receiving desmopressinJ C Smith, H A Lane, J Lewis, et al.Pageof 94