Copy Number Variation in CCND1 Gene Is Implicated in the Pathogenesis of Sporadic Parathyroid Carcinoma
Published 2014 View Full Article
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Title
Copy Number Variation in CCND1 Gene Is Implicated in the Pathogenesis of Sporadic Parathyroid Carcinoma
Authors
Keywords
Parathyroid Adenoma, Parathyroid Carcinoma, Parathyroid Tumor, PHPT Patient, CCND1 Gene
Journal
WORLD JOURNAL OF SURGERY
Volume 38, Issue 7, Pages 1730-1737
Publisher
Springer Nature
Online
2014-02-08
DOI
10.1007/s00268-014-2455-9
References
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- (2012) A. J. Rogers et al. CLINICAL AND EXPERIMENTAL ALLERGY
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- (2011) P. V. Pradeep et al. International Journal of Endocrinology
- ESR1 amplification is rare in breast cancer and is associated with high grade and high proliferation: a multiplex ligation-dependent probe amplification study
- (2011) Cathy B. Moelans et al. CELLULAR ONCOLOGY
- Parathyroid carcinoma: a 16-year experience in a single institution
- (2010) Yong Sang Lee et al. ENDOCRINE JOURNAL
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- (2009) HuiYing Jia et al. HUMAN PATHOLOGY
- Hyperparathyroidism
- (2009) William D Fraser LANCET
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