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Ishida, T, Yokoe, T, Sensyou, M. Domestic report of parathyroid tumor (cases of 1980-1989). Endocine Surgery 1991;8: 37\u201345(In Japanese)."},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Cetani, F, Pardi, E, Borsari, S, Viacava, P, Dipollina, G, Cianferotti, L, et al. Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors. J Clin Endocrinol Metab 2004;89: 5583\u201391.","DOI":"10.1210\/jc.2004-0294"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Simonds, WF, Robbins, CM, Agarwal, SK, Hendy, GN, Carpten, JD, Marx, SJ. Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome. J Clin Endocrinol Metab 2004;89: 96\u2013102.","DOI":"10.1210\/jc.2003-030675"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Kollars, J, Zarroug, AE, van Heerden, J, Lteif, A, Stavlo, P, Suarez, L, et al. Primary hyperparathyroidism in pediatric patients. Pediatrics 2005;115: 974\u201380.","DOI":"10.1542\/peds.2004-0804"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Mizusawa, N, Uchino, S, Iwata, T, Tsuyuguchi, M, Suzuki, Y, Mizukoshi, T, et al. Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome. Clin Endocrinol (Oxf) 2006;65: 9\u201316.","DOI":"10.1111\/j.1365-2265.2006.02534.x"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Yamashita, Y, Akiyama, T, Mizusawa, N, Yoshimoto, K, Goto, M. A case of hyperparathyroidism-jaw tumour syndrome found in the treatment of an ossifying fibroma in the maxillary bone. Int J Oral Maxillofac Surg 2007;36: 365\u20139.","DOI":"10.1016\/j.ijom.2006.08.007"},{"key":"7","unstructured":"7. Teh, BT, Farnebo, F, Kristoffersson, U, Sundelin, B, Cardinal, J, Axelson, R, et al. Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas. J Clin Endocrinol Metab 1996;81: 4204\u201311."},{"key":"8","unstructured":"8. Szab\u00f3, J, Heath, B, Hill, VM, Jackson, CE, Zarbo, RJ, Mallette, LE, et al. Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31. Am J Hum Genet 1995;56: 944\u201350."},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Schmidt, BP, Bradrick, JP, Gabali, A. Hyperparathyroidism-jaw tumor syndrome: a case report. J Oral Maxillofac Surg 2009;67: 423\u20137.","DOI":"10.1016\/j.joms.2008.07.015"},{"key":"10","unstructured":"10. Mizukoshi, T, Sato, H, Takahashi, Y, Imai, K, Suzuki, Y, Uchino, S, et al. ( 2006) A case of familial isolated hyperparathyroidism with <i>HRPT2<\/i> mutation. <i>Nihon Naibunpitsugakkai zasshi<\/i> 2006;82: 42\u20135 (In Japanese)."},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Iacobone, M, Masi, G, Barzon, L, Porzionato, A, Macchi, V, Ciarleglio, FA, et al. Hyperparathyroidism-jaw tumor syndrome: a report of three large kindred. Langenbecks Arch Surg 2009;394: 817\u201325.","DOI":"10.1007\/s00423-009-0511-y"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Kutcher, MR, Rigby, MH, Bullock, M, Trites, J, Taylor, SM, Hart, RD. Hyperparathyroidism-jaw tumor syndrome. Head Neck 2013;35: E175\u20137.","DOI":"10.1002\/hed.22918"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Kelly, TG, Shattuck, TM, Reyes-Mugica, M, Stewart, AF, Simonds, WF, Udelsman, R, et al. Surveillance for early detection of aggressive parathyroid disease: carcinoma and atypical adenoma in familial isolated hyperparathyroidism associated with a germline HRPT2 mutation. J Bone Miner Res 2006;21: 1666\u201371.","DOI":"10.1359\/jbmr.060702"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Bradley, KJ, Cavaco, BM, Bowl, MR, Harding, B, Cranston, T, Fratter, C, et al. Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours. Clin Endocrinol (Oxf) 2006;64: 299\u2013306.","DOI":"10.1111\/j.1365-2265.2006.02460.x"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Newey, PJ, Bowl, MR, Cranston, T, Thakker, RV. Cell division cycle protein 73 homolog (<i>CDC73<\/i>) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors. Hum Mutat 2010;31: 295\u2013307.","DOI":"10.1002\/humu.21188"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Woodard, GE, Lin, L, Zhang, JH, Agarwal, SK, Marx, SJ, Simonds, WF. Parafibromin, product of the hyperparathyroidism-jaw tumor syndrome gene <i>HRPT2<\/i>, regulates cyclin D1\/PRAD1 expression. Oncogene 2005;24: 1272\u20136.","DOI":"10.1038\/sj.onc.1208274"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Yart, A, Gstaiger, M, Wirbelauer, C, Pecnik, M, Anastasiou, D, Hess, D, et al. The <i>HRPT2<\/i> tumor suppressor gene product parafibromin associates with human PAF1 and RNA polymerase II. Mol Cell Biol 2005;25: 5052\u201360.","DOI":"10.1128\/MCB.25.12.5052-5060.2005"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Cui, C, Lal, P, Master, S, Ma, Y, Baradet, T, Bing, Z. Expression of parafibromin in major renal cell tumors. Eur J Histochem 2012;56: e39.","DOI":"10.4081\/ejh.2012.e39"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. Carpten, JD, Robbins, CM, Villablanca, A, Forsberg, L, Presciuttini, S, Bailey-Wilson, J, et al. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nat Genet 2002;32: 676\u201380.","DOI":"10.1038\/ng1048"},{"key":"20","doi-asserted-by":"crossref","unstructured":"20. Sharretts, JM, Simonds, WF. Clinical and molecular genetics of parathyroid neoplasms. Best Pract Res Clin Endocrinol Metab 2010;24: 491\u2013502.","DOI":"10.1016\/j.beem.2010.01.003"},{"key":"21","doi-asserted-by":"crossref","unstructured":"21. Udelsman, R, \u00c5kerstr\u00f6m, G, Biagini, C, Duh, QY, Miccoli, P, Niederle, B, et al. The surgical management of asymptomatic primary hyperparathyroidism: proceedings of the Fourth International Workshop. 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