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Journal of the American Academy of Dermatology|September 16, 2009
Selection criteria for genetic assessment of patients with familial melanomaSancy A Leachman, John Carucci, Wendy Kohlmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2004
Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient miceMark Veugelers, David Wilkes, Kimberly Burton, et al.
British Journal of Cancer|January 31, 2013
Common genetic variants in the 9p21 region and their associations with multiple tumoursF Gu, R M Pfeiffer, S Bhattacharjee, et al.
Nature Genetics|August 24, 2010
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinomaChristian C Abnet, Neal D Freedman, Nan Hu, et al.
Medrxiv : the Preprint Server for Health Sciences|June 12, 2026
Disruption of CTCF binding by germline non-coding variants in CDKN2B suppress CDKN2A expression and predispose to melanomaJessica L Scales, Jayne A Barbour, Alisa M Goldstein, et al.
Journal of Medical Genetics|August 15, 2006
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continentsAlisa M Goldstein, May Chan, Mark Harland, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 16, 2017
International cancer seminars: a focus on esophageal squamous cell carcinomaG Murphy, V McCormack, B Abedi-Ardekani, et al.
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