Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas

CONTEXT: Genetic abnormalities, such as those of multiple endocrine neoplasia type 1 (MEN1) and Cyclin D1 (CCND1) genes, occur in <50% of nonhereditary (sporadic) parathyroid adenomas. OBJECTIVE: To identify genetic abnormalities in nonhereditary parathyroid adenomas by whole-exome sequence analy...

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Опубликовано в: :J Clin Endocrinol Metab
Главные авторы: Newey, Paul J., Nesbit, M. Andrew, Rimmer, Andrew J., Attar, Moustafa, Head, Rosie T., Christie, Paul T., Gorvin, Caroline M., Stechman, Michael, Gregory, Lorna, Mihai, Radu, Sadler, Greg, McVean, Gil, Buck, David, Thakker, Rajesh V.
Формат: Artigo
Язык:Inglês
Опубликовано: Endocrine Society 2012
Предметы:
JCEM Online: Advances in Genetics
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4446457/
https://ncbi.nlm.nih.gov/pubmed/22855342
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2012-2303
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