{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,28]],"date-time":"2026-08-28T12:40:24Z","timestamp":1787920824213,"version":"build-2784847793"},"reference-count":41,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[2013,2,24]],"date-time":"2013-02-24T00:00:00Z","timestamp":1361664000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Endocrine"],"published-print":{"date-parts":[[2013,10]]},"DOI":"10.1007\/s12020-013-9903-4","type":"journal-article","created":{"date-parts":[[2013,2,23]],"date-time":"2013-02-23T17:13:24Z","timestamp":1361639604000},"page":"489-495","source":"Crossref","is-referenced-by-count":29,"title":["Allelic imbalance in sporadic parathyroid carcinoma and evidence for its de novo origins"],"prefix":"10.1007","volume":"44","author":[{"given":"Jessica","family":"Costa-Guda","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yasuo","family":"Imanishi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nallasivam","family":"Palanisamy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Norihiko","family":"Kawamata","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H.","family":"Phillip Koeffler","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R. S. K.","family":"Chaganti","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrew","family":"Arnold","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2013,2,24]]},"reference":[{"issue":"12","key":"9903_CR1","doi-asserted-by":"crossref","first-page":"1869","DOI":"10.1359\/jbmr.081018","volume":"23","author":"C Marcocci","year":"2008","unstructured":"C. Marcocci, F. Cetani, M.R. Rubin, S.J. Silverberg, A. Pinchera, J.P. Bilezikian, Parathyroid carcinoma. J. Bone Miner. Res. 23(12), 1869\u20131880 (2008)","journal-title":"J. Bone Miner. Res."},{"key":"9903_CR2","first-page":"103","volume-title":"Endocrine Pathology","author":"RL Apel","year":"2002","unstructured":"R.L. Apel, S.L. Asa, The Parathyroid Glands, in Endocrine pathology, ed. by V. LiVolsi, S. Asa (Churchill Livingstone, Philadelphia, 2002), pp. 103\u2013147"},{"issue":"2","key":"9903_CR3","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1210\/jc.86.2.485","volume":"86","author":"E Shane","year":"2001","unstructured":"E. Shane, Clinical review 122: parathyroid carcinoma. J. Clin. Endocrinol. Metab. 86(2), 485\u2013493 (2001)","journal-title":"J. Clin. Endocrinol. Metab."},{"issue":"4901","key":"9903_CR4","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1126\/science.2565047","volume":"244","author":"B Vogelstein","year":"1989","unstructured":"B. Vogelstein, E.R. Fearon, S.E. Kern, S.R. Hamilton, A.C. Preisinger, Y. Nakamura, R. White, Allelotype of colorectal carcinomas. Science 244(4901), 207\u2013211 (1989)","journal-title":"Science"},{"key":"9903_CR5","doi-asserted-by":"crossref","first-page":"397","DOI":"10.1016\/B978-0-12-387829-8.00025-1","volume-title":"Genetics of Bone Biology and Skeletal Disease","author":"J Costa-Guda","year":"2013","unstructured":"J. Costa-Guda, A. Arnold, Hyperparathyroidism, in Genetics of bone biology and skeletal disease, ed. by R.V. Thakker, M.P. Whyte, J.A. Eisman, T. Igarashi (Academic Press, San Diego, 2013), pp. 397\u2013408"},{"issue":"6318","key":"9903_CR6","doi-asserted-by":"crossref","first-page":"512","DOI":"10.1038\/350512a0","volume":"350","author":"T Motokura","year":"1991","unstructured":"T. Motokura, T. Bloom, H.G. Kim, H. Juppner, J.V. Ruderman, H.M. Kronenberg, A. Arnold, A novel cyclin encoded by a bcl1-linked candidate oncogene. Nature 350(6318), 512\u2013515 (1991)","journal-title":"Nature"},{"issue":"6","key":"9903_CR7","first-page":"543","volume":"43","author":"A Arnold","year":"1995","unstructured":"A. Arnold, The cyclin D1\/PRAD1 oncogene in human neoplasia. J. Investig. Med. 43(6), 543\u2013549 (1995)","journal-title":"J. Investig. Med."},{"issue":"5","key":"9903_CR8","doi-asserted-by":"crossref","first-page":"1736","DOI":"10.1210\/jc.81.5.1736","volume":"81","author":"ED Hsi","year":"1996","unstructured":"E.D. Hsi, L.R. Zukerberg, W.I. Yang, A. Arnold, Cyclin D1\/PRAD1 expression in parathyroid adenomas: an immunohistochemical study. J. Clin. Endocrinol. Metab. 81(5), 1736\u20131739 (1996)","journal-title":"J. Clin. Endocrinol. Metab."},{"issue":"5311","key":"9903_CR9","doi-asserted-by":"crossref","first-page":"404","DOI":"10.1126\/science.276.5311.404","volume":"276","author":"SC Chandrasekharappa","year":"1997","unstructured":"S.C. Chandrasekharappa, S.C. Guru, P. Manickam, S.E. Olufemi, F.S. Collins, M.R. Emmert-Buck, L.V. Debelenko, Z. Zhuang, I.A. Lubensky, L.A. Liotta, J.S. Crabtree, Y. Wang, B.A. Roe, J. Weisemann, M.S. Boguski, S.K. Agarwal, M.B. Kester, Y.S. Kim, C. Heppner, Q. Dong, A.M. Spiegel, A.L. Burns, S.J. Marx, Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science 276(5311), 404\u2013407 (1997)","journal-title":"Science"},{"issue":"4","key":"9903_CR10","doi-asserted-by":"crossref","first-page":"E701","DOI":"10.1210\/jc.2010-1338","volume":"96","author":"J Costa-Guda","year":"2011","unstructured":"J. Costa-Guda, I. Marinoni, S. Molatore, N.S. Pellegata, A. Arnold, Somatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomas. J. Clin. Endocrinol. Metab. 96(4), E701\u2013E706 (2011)","journal-title":"J. Clin. Endocrinol. Metab."},{"issue":"42","key":"9903_CR11","doi-asserted-by":"crossref","first-page":"15558","DOI":"10.1073\/pnas.0603877103","volume":"103","author":"NS Pellegata","year":"2006","unstructured":"N.S. Pellegata, L. Quintanilla-Martinez, H. Siggelkow, E. Samson, K. Bink, H. Hofler, F. Fend, J. Graw, M.J. Atkinson, Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans. Proc Natl Acad Sci USA 103(42), 15558\u201315563 (2006)","journal-title":"Proc Natl Acad Sci USA"},{"issue":"5","key":"9903_CR12","doi-asserted-by":"crossref","first-page":"1826","DOI":"10.1210\/jc.2008-2083","volume":"94","author":"SK Agarwal","year":"2009","unstructured":"S.K. Agarwal, C.M. Mateo, S.J. Marx, Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states. J. Clin. Endocrinol. Metab. 94(5), 1826\u20131834 (2009)","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"9903_CR13","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1186\/1476-4598-7-53","volume":"7","author":"P Bjorklund","year":"2008","unstructured":"P. Bjorklund, D. Lindberg, G. Akerstrom, G. Westin, Stabilizing mutation of CTNNB1\/beta-catenin and protein accumulation analyzed in a large series of parathyroid tumors of Swedish patients. Mol. Cancer 7, 53 (2008)","journal-title":"Mol. Cancer"},{"issue":"1","key":"9903_CR14","doi-asserted-by":"crossref","first-page":"152","DOI":"10.1007\/s12020-011-9558-y","volume":"41","author":"V Guarnieri","year":"2012","unstructured":"V. Guarnieri, F. Baorda, C. Battista, M. Bisceglia, T. Balsamo, E. Gruppioni, M. Fiorentino, L.A. Muscarella, M. Coco, R. Barbano, S. Corbetta, A. Spada, D.E. Cole, L. Canaff, G.N. Hendy, M. Carella, A. Scillitani, A rare S33C mutation of CTNNB1 encoding beta-catenin in a parathyroid adenoma found in an Italian primary hyperparathyroid cohort. Endocrine 41(1), 152\u2013155 (2012). doi: 10.1007\/s12020-011-9558-y","journal-title":"Endocrine"},{"issue":"3","key":"9903_CR15","doi-asserted-by":"crossref","first-page":"612","DOI":"10.1007\/s12020-012-9690-3","volume":"42","author":"LF Starker","year":"2012","unstructured":"L.F. Starker, A. Fonseca, G. Akerstrom, P. Bjorklund, G. Westin, T. Carling, Evidence of a stabilizing mutation of beta-catenin encoded by CTNNB1 exon 3 in a large series of sporadic parathyroid adenomas. Endocrine 42(3), 612\u2013615 (2012). doi: 10.1007\/s12020-012-9690-3","journal-title":"Endocrine"},{"issue":"9","key":"9903_CR16","doi-asserted-by":"crossref","first-page":"E1774","DOI":"10.1210\/jc.2012-1743","volume":"97","author":"MK Cromer","year":"2012","unstructured":"M.K. Cromer, L.F. Starker, M. Choi, R. Udelsman, C. Nelson-Williams, R.P. Lifton, T. Carling, Identification of somatic mutations in parathyroid tumors using whole-exome sequencing. J. Clin. Endocrinol. Metab. 97(9), E1774\u2013E1781 (2012). doi: 10.1210\/jc.2012-1743","journal-title":"J. Clin. Endocrinol. Metab."},{"issue":"10","key":"9903_CR17","doi-asserted-by":"crossref","first-page":"E1995","DOI":"10.1210\/jc.2012-2303","volume":"97","author":"PJ Newey","year":"2012","unstructured":"P.J. Newey, M.A. Nesbit, A.J. Rimmer, M. Attar, R.T. Head, P.T. Christie, C.M. Gorvin, M. Stechman, L. Gregory, R. Mihai, G. Sadler, G. McVean, D. Buck, R.V. Thakker, Whole-exome sequencing studies of nonhereditary (sporadic) parathyroid adenomas. J. Clin. Endocrinol. Metab. 97(10), E1995\u2013E2005 (2012). doi: 10.1210\/jc.2012-2303","journal-title":"J. Clin. Endocrinol. Metab."},{"issue":"18","key":"9903_CR18","doi-asserted-by":"crossref","first-page":"1722","DOI":"10.1056\/NEJMoa031237","volume":"349","author":"TM Shattuck","year":"2003","unstructured":"T.M. Shattuck, S. Valimaki, T. Obara, R.D. Gaz, O.H. Clark, D. Shoback, M.E. Wierman, K. Tojo, C.M. Robbins, J.D. Carpten, L.O. Farnebo, C. Larsson, A. Arnold, Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma. N. Engl. J. Med. 349(18), 1722\u20131729 (2003)","journal-title":"N. Engl. J. Med."},{"issue":"11","key":"9903_CR19","doi-asserted-by":"crossref","first-page":"5583","DOI":"10.1210\/jc.2004-0294","volume":"89","author":"F Cetani","year":"2004","unstructured":"F. Cetani, E. Pardi, S. Borsari, P. Viacava, G. Dipollina, L. Cianferotti, E. Ambrogini, E. Gazzerro, G. Colussi, P. Berti, P. Miccoli, A. Pinchera, C. Marcocci, Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors. J. Clin. Endocrinol. Metab. 89(11), 5583\u20135591 (2004)","journal-title":"J. Clin. Endocrinol. Metab."},{"issue":"9","key":"9903_CR20","doi-asserted-by":"crossref","first-page":"657","DOI":"10.1136\/jmg.40.9.657","volume":"40","author":"VM Howell","year":"2003","unstructured":"V.M. Howell, C.J. Haven, K. Kahnoski, S.K. Khoo, D. Petillo, J. Chen, G.J. Fleuren, B.G. Robinson, L.W. Delbridge, J. Philips, A.E. Nelson, U. Krause, K. Hammje, H. Dralle, C. Hoang-Vu, O. Gimm, D.J. Marsh, H. Morreau, B.T. Teh, HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. J. Med. Genet. 40(9), 657\u2013663 (2003)","journal-title":"J. Med. Genet."},{"issue":"9","key":"9903_CR21","doi-asserted-by":"crossref","first-page":"5015","DOI":"10.1210\/jc.2005-0717","volume":"90","author":"LJ Krebs","year":"2005","unstructured":"L.J. Krebs, T.M. Shattuck, A. Arnold, HRPT2 mutational analysis of typical sporadic parathyroid adenomas. J. Clin. Endocrinol. Metab. 90(9), 5015\u20135017 (2005)","journal-title":"J. Clin. Endocrinol. Metab."},{"issue":"6","key":"9903_CR22","doi-asserted-by":"crossref","first-page":"634","DOI":"10.1046\/j.1365-2796.2003.01168.x","volume":"253","author":"JD Chen","year":"2003","unstructured":"J.D. Chen, C. Morrison, C. Zhang, K. Kahnoski, J.D. Carpten, B.T. Teh, Hyperparathyroidism-jaw tumour syndrome. J. Intern. Med. 253(6), 634\u2013642 (2003)","journal-title":"J. Intern. Med."},{"issue":"1","key":"9903_CR23","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1111\/j.1365-2796.2004.01421.x","volume":"257","author":"KJ Bradley","year":"2005","unstructured":"K.J. Bradley, M.R. Hobbs, I.D. Buley, J.D. Carpten, B.M. Cavaco, J.E. Fares, P. Laidler, S. Manek, C.M. Robbins, I.S. Salti, N.W. Thompson, C.E. Jackson, R.V. Thakker, Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome. J. Intern. Med. 257(1), 18\u201326 (2005). doi: 10.1111\/j.1365-2796.2004.01421.x","journal-title":"J. Intern. Med."},{"key":"9903_CR24","first-page":"495","volume":"73","author":"SI Roth","year":"1962","unstructured":"S.I. Roth, Pathology of the parathyroids in hyperparathyroidism. Discussion of recent advances in the anatomy and pathology of the parathyroid glands. Arch. Pathol. 73, 495\u2013510 (1962)","journal-title":"Arch. Pathol."},{"issue":"14","key":"9903_CR25","doi-asserted-by":"crossref","first-page":"6071","DOI":"10.1158\/0008-5472.CAN-05-0465","volume":"65","author":"Y Nannya","year":"2005","unstructured":"Y. Nannya, M. Sanada, K. Nakazaki, N. Hosoya, L. Wang, A. Hangaishi, M. Kurokawa, S. Chiba, D.K. Bailey, G.C. Kennedy, S. Ogawa, A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. Cancer Res. 65(14), 6071\u20136079 (2005)","journal-title":"Cancer Res."},{"issue":"5","key":"9903_CR26","doi-asserted-by":"crossref","first-page":"1766","DOI":"10.1210\/jc.83.5.1766","volume":"83","author":"N Palanisamy","year":"1998","unstructured":"N. Palanisamy, Y. Imanishi, P.H. Rao, H. Tahara, R.S. Chaganti, A. Arnold, Novel chromosomal abnormalities identified by comparative genomic hybridization in parathyroid adenomas. J. Clin. Endocrinol. Metab. 83(5), 1766\u20131770 (1998)","journal-title":"J. Clin. Endocrinol. Metab."},{"issue":"8","key":"9903_CR27","doi-asserted-by":"crossref","first-page":"3911","DOI":"10.1210\/jc.87.8.3911","volume":"87","author":"TM Shattuck","year":"2002","unstructured":"T.M. Shattuck, J. Costa, M. Bernstein, R.T. Jensen, D.C. Chung, A. Arnold, Mutational analysis of Smad3, a candidate tumor suppressor implicated in TGF-beta and menin pathways, in parathyroid adenomas and enteropancreatic endocrine tumors. J. Clin. Endocrinol. Metab. 87(8), 3911\u20133914 (2002)","journal-title":"J. Clin. Endocrinol. Metab."},{"issue":"2","key":"9903_CR28","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1002\/1097-0142(19820115)49:2<388::AID-CNCR2820490230>3.0.CO;2-F","volume":"49","author":"KA Aldinger","year":"1982","unstructured":"K.A. Aldinger, R.C. Hickey, M.L. Ibanez, N.A. Samaan, Parathyroid carcinoma: a clinical study of seven cases of functioning and two cases of nonfunctioning parathyroid cancer. Cancer 49(2), 388\u2013397 (1982)","journal-title":"Cancer"},{"issue":"3","key":"9903_CR29","first-page":"154","volume":"18","author":"Y Berland","year":"1982","unstructured":"Y. Berland, M. Olmer, G. Lebreuil, J. Grisoli, Parathyroid carcinoma, adenoma and hyperplasia in a case of chronic renal insufficiency on dialysis. Clin. Nephrol. 18(3), 154\u2013158 (1982)","journal-title":"Clin. Nephrol."},{"issue":"1","key":"9903_CR30","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1016\/0002-9343(84)90447-9","volume":"77","author":"CE Desch","year":"1984","unstructured":"C.E. Desch, G. Arsensis, P.D. Woolf, A.G. May, J.M. Amatruda, Parathyroid hyperplasia and carcinoma within one gland. Am. J. Med. 77(1), 131\u2013134 (1984)","journal-title":"Am. J. Med."},{"issue":"7","key":"9903_CR31","first-page":"349","volume":"107","author":"P Haghighi","year":"1983","unstructured":"P. Haghighi, R.W. Astarita, H.T. Wepsic, P.L. Wolf, Concurrent primary parathyroid hyperplasia and parathyroid carcinoma. Arch. Pathol. Lab. Med. 107(7), 349\u2013350 (1983)","journal-title":"Arch. Pathol. Lab. Med."},{"issue":"1 Pt 1","key":"9903_CR32","doi-asserted-by":"crossref","first-page":"126","DOI":"10.1016\/S0022-5347(17)57920-3","volume":"118","author":"T Murayama","year":"1977","unstructured":"T. Murayama, K. Kawabe, M. Tagami, A case of parathyroid carcinoma concurred with hyperplasia: an electron microscopic study. J. Urol. 118(1 Pt 1), 126\u2013127 (1977)","journal-title":"J. Urol."},{"issue":"1","key":"9903_CR33","doi-asserted-by":"crossref","first-page":"30","DOI":"10.1016\/S0165-4608(98)00049-1","volume":"106","author":"SK Agarwal","year":"1998","unstructured":"S.K. Agarwal, E. Schrock, M.B. Kester, A.L. Burns, C.S. Heffess, T. Ried, S.J. Marx, Comparative genomic hybridization analysis of human parathyroid tumors. Cancer Genet. Cytogenet. 106(1), 30\u201336 (1998)","journal-title":"Cancer Genet. Cytogenet."},{"key":"9903_CR34","unstructured":"J. Costa-Guda, E. H. Samander, A. Arnold, Loss of heterozygosity analysis of parathyroid adenomas by single nucleotide polymorphism arrays. Paper presented at the Proceedings of the Annual Meeting of the American Association for Cancer Research"},{"issue":"10","key":"9903_CR35","doi-asserted-by":"crossref","first-page":"3775","DOI":"10.1210\/jc.84.10.3775","volume":"84","author":"F Farnebo","year":"1999","unstructured":"F. Farnebo, S. Kytola, B.T. Teh, T. Dwight, F.K. Wong, A. Hoog, M. Elvius, W.S. Wassif, N.W. Thompson, L.O. Farnebo, K. Sandelin, C. Larsson, Alternative genetic pathways in parathyroid tumorigenesis. J. Clin. Endocrinol. Metab. 84(10), 3775\u20133780 (1999)","journal-title":"J. Clin. Endocrinol. Metab."},{"issue":"8","key":"9903_CR36","doi-asserted-by":"crossref","first-page":"1049","DOI":"10.1097\/01.pas.0000166368.68459.99","volume":"29","author":"JL Hunt","year":"2005","unstructured":"J.L. Hunt, S.E. Carty, J.H. Yim, J. Murphy, L. Barnes, Allelic loss in parathyroid neoplasia can help characterize malignancy. Am. J. Surg. Pathol. 29(8), 1049\u20131055 (2005)","journal-title":"Am. J. Surg. Pathol."},{"issue":"3","key":"9903_CR37","first-page":"599","volume":"56","author":"H Tahara","year":"1996","unstructured":"H. Tahara, A.P. Smith, R.D. Gas, V.L. Cryns, A. Arnold, Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas. Cancer Res. 56(3), 599\u2013605 (1996)","journal-title":"Cancer Res."},{"issue":"2","key":"9903_CR38","doi-asserted-by":"crossref","first-page":"579","DOI":"10.1016\/S0002-9440(10)64568-3","volume":"157","author":"S Kytola","year":"2000","unstructured":"S. Kytola, F. Farnebo, T. Obara, J. Isola, L. Grimelius, L.O. Farnebo, K. Sandelin, C. Larsson, Patterns of chromosomal imbalances in parathyroid carcinomas. Am. J. Pathol. 157(2), 579\u2013586 (2000)","journal-title":"Am. J. Pathol."},{"issue":"2","key":"9903_CR39","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1210\/jc.2008-1762","volume":"94","author":"A Khan","year":"2009","unstructured":"A. Khan, A. Grey, D. Shoback, Medical management of asymptomatic primary hyperparathyroidism: proceedings of the third international workshop. J. Clin. Endocrinol. Metab. 94(2), 373\u2013381 (2009). doi: 10.1210\/jc.2008-1762","journal-title":"J. Clin. Endocrinol. Metab."},{"issue":"4","key":"9903_CR40","doi-asserted-by":"crossref","first-page":"676","DOI":"10.1038\/ng1048","volume":"32","author":"JD Carpten","year":"2002","unstructured":"J.D. Carpten, C.M. Robbins, A. Villablanca, L. Forsberg, S. Presciuttini, J. Bailey-Wilson, W.F. Simonds, E.M. Gillanders, A.M. Kennedy, J.D. Chen, S.K. Agarwal, R. Sood, M.P. Jones, T.Y. Moses, C. Haven, D. Petillo, P.D. Leotlela, B. Harding, D. Cameron, A.A. Pannett, A. Hoog, H. Heath 3rd, L.A. James-Newton, B. Robinson, R.J. Zarbo, B.M. Cavaco, W. Wassif, N.D. Perrier, I.B. Rosen, U. Kristoffersson, P.D. Turnpenny, L.O. Farnebo, G.M. Besser, C.E. Jackson, H. Morreau, J.M. Trent, R.V. Thakker, S.J. Marx, B.T. Teh, C. Larsson, M.R. Hobbs, HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nat. Genet. 32(4), 676\u2013680 (2002)","journal-title":"Nat. Genet."},{"issue":"8","key":"9903_CR41","doi-asserted-by":"crossref","first-page":"2827","DOI":"10.1210\/jc.2005-1239","volume":"91","author":"V Guarnieri","year":"2006","unstructured":"V. Guarnieri, A. Scillitani, L.A. Muscarella, C. Battista, N. Bonfitto, M. Bisceglia, S. Minisola, M.L. Mascia, L. D\u2019Agruma, D.E. Cole, Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: implications for cancer surveillance. J. Clin. Endocrinol. Metab. 91(8), 2827\u20132832 (2006)","journal-title":"J. Clin. Endocrinol. Metab."}],"container-title":["Endocrine"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s12020-013-9903-4.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s12020-013-9903-4\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s12020-013-9903-4","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,2,9]],"date-time":"2022-02-09T10:35:12Z","timestamp":1644402912000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s12020-013-9903-4"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,2,24]]},"references-count":41,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2013,10]]}},"alternative-id":["9903"],"URL":"https:\/\/doi.org\/10.1007\/s12020-013-9903-4","relation":{},"ISSN":["1355-008X","1559-0100"],"issn-type":[{"value":"1355-008X","type":"print"},{"value":"1559-0100","type":"electronic"}],"subject":[],"published":{"date-parts":[[2013,2,24]]}}}