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Items: 7

1.

Familial hyperparathyroidism due to a germline mutation of the CDC73 gene: implications for management and age-appropriate testing of relatives at risk.

Pichardo-Lowden AR, Manni A, Saunders BD, Baker MJ.

Endocr Pract. 2011 Jul-Aug;17(4):602-9. doi: 10.4158/EP10337.RA. Review.

PMID:
21324824
2.

Tumor suppressor gene mutation in a patient with a history of hyperparathyroidism-jaw tumor syndrome and healed generalized osteitis fibrosa cystica: a case report and genetic pathophysiology review.

Parfitt J, Harris M, Wright JM, Kalamchi S.

J Oral Maxillofac Surg. 2015 Jan;73(1):194.e1-9. doi: 10.1016/j.joms.2014.09.008. Epub 2014 Sep 28. Review.

PMID:
25511968
3.

A germline mutation of HRPT2/CDC73 (70 G>T) in an adolescent female with parathyroid carcinoma: first case report and a review of the literature.

Serrano-Gonzalez M, Shay S, Austin J, Maceri DR, Pitukcheewanont P.

J Pediatr Endocrinol Metab. 2016 Sep 1;29(9):1005-12. doi: 10.1515/jpem-2016-0109. Review.

4.

HRPT2, a tumor suppressor gene for hyperparathyroidism-jaw tumor syndrome.

Wang PF, Tan MH, Zhang C, Morreau H, Teh BT.

Horm Metab Res. 2005 Jun;37(6):380-3. Review.

PMID:
16001331
5.

Scoping the family history: assessment of Lynch syndrome (hereditary nonpolyposis colorectal cancer) in primary care settings--a primer for nurse practitioners.

Maradiegue A, Jasperson K, Edwards QT, Lowstuter K, Weitzel J.

J Am Acad Nurse Pract. 2008 Feb;20(2):76-84. doi: 10.1111/j.1745-7599.2007.00282.x. Review.

PMID:
18271762
6.

Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds.

Simonds WF, James-Newton LA, Agarwal SK, Yang B, Skarulis MC, Hendy GN, Marx SJ.

Medicine (Baltimore). 2002 Jan;81(1):1-26. Review. No abstract available.

7.

Genetics of primary hyperparathyroidism.

Brandi ML, Falchetti A.

Urol Int. 2004;72 Suppl 1:11-6. Review.

PMID:
15133326

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