Showing results (71-80 of 318) with videos related to
Sort By:
Pageof 32
American Journal of Medical Genetics|September 1, 1992
Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defectsN M Lindor, V V Michels, D A Hoppe, et al.Human Molecular Genetics|April 25, 2002
Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorderCarol A Wise, Joseph D Gillum, Christine E Seidman, et al.Cancer Genetics and Cytogenetics|July 2, 1998
Search for chromosome instability in lymphocytes with germ-line mutations in DNA mismatch repair genesN M Lindor, S M Jalal, T J VanDeWalker, et al.Gastroenterology|October 31, 1998
Familial predisposition for colorectal cancer in chronic ulcerative colitis: a case-control studyK W Nuako, D A Ahlquist, D W Mahoney, et al.Oncotarget|December 8, 2017
Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry CohortLeon Raskin, Yan Guo, Liping Du, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2021
Penetrance and outcomes at 1-year following return of actionable variants identified by genome sequencingChristopher Lee, Omar Elsekaily, David C Kochan, et al.American Journal of Medical Genetics|May 26, 1999
Guidelines for buccal smear collection in breast-fed infantsD Babovic-Vuksanovic, V V Michels, M E Law, et al.Cancer|March 11, 2003
Frequency of loss of hMLH1 expression in colorectal carcinoma increases with advancing ageSanjay Kakar, Lawrence J Burgart, Stephen N Thibodeau, et al.Human Heredity|March 17, 1999
Hereditary desmoid disease in a family with a germline Alu I repeat mutation of the APC geneK C Halling, C R Lazzaro, R Honchel, et al.American Journal of Medical Genetics|June 1, 1993
Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophyS M Jalal, N M Lindor, V V Michels, et al.Pageof 32