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

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Bibliographic Details
Published in:The journal of clinical endocrinology and metabolism 2012-10, Vol.97 (10), p.E1995-E2005
Main Authors: 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
Format: Article
Language:English
Subjects:
Adenoma - genetics
Aged
Aged, 80 and over
Cyclin D1 - genetics
DNA Mutational Analysis - methods
Exome - genetics
Female
Genetic Variation - genetics
Humans
Hyperparathyroidism, Primary - genetics
JCEM Online: Advances in Genetics
Male
Middle Aged
Multiple Endocrine Neoplasia Type 1 - genetics
Parathyroid Neoplasms - genetics
Shelterin Complex
Telomere-Binding Proteins - genetics
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Description
Summary:Context: Genetic abnormalities, such as those of multiple endocrine neoplasia type 1 (MEN1) and Cyclin D1 (CCND1) genes, occur in
ISSN:0021-972X
1945-7197
DOI:10.1210/jc.2012-2303