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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1973 1
1995 2
1998 5
1999 2
2000 4
2001 1
2002 4
2003 4
2004 11
2005 6
2006 8
2007 6
2008 5
2010 2
2011 4
2012 3
2013 3
2014 2
2015 1
2017 1
2018 1
2019 2
2021 1
2022 2
2023 1
2024 0

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Similar articles for PMID: 14985403

76 results

Results by year

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Page 1
Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP).
Villablanca A, Calender A, Forsberg L, Höög A, Cheng JD, Petillo D, Bauters C, Kahnoski K, Ebeling T, Salmela P, Richardson AL, Delbridge L, Meyrier A, Proye C, Carpten JD, Teh BT, Robinson BG, Larsson C. Villablanca A, et al. J Med Genet. 2004 Mar;41(3):e32. doi: 10.1136/jmg.2003.012369. J Med Genet. 2004. PMID: 14985403 Free PMC article. No abstract available.
Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome.
Mizusawa N, Uchino S, Iwata T, Tsuyuguchi M, Suzuki Y, Mizukoshi T, Yamashita Y, Sakurai A, Suzuki S, Beniko M, Tahara H, Fujisawa M, Kamata N, Fujisawa K, Yashiro T, Nagao D, Golam HM, Sano T, Noguchi S, Yoshimoto K. Mizusawa N, et al. Clin Endocrinol (Oxf). 2006 Jul;65(1):9-16. doi: 10.1111/j.1365-2265.2006.02534.x. Clin Endocrinol (Oxf). 2006. PMID: 16817812
HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours.
Howell VM, Haven CJ, Kahnoski K, Khoo SK, Petillo D, Chen J, Fleuren GJ, Robinson BG, Delbridge LW, Philips J, Nelson AE, Krause U, Hammje K, Dralle H, Hoang-Vu C, Gimm O, Marsh DJ, Morreau H, Teh BT. Howell VM, et al. J Med Genet. 2003 Sep;40(9):657-63. doi: 10.1136/jmg.40.9.657. J Med Genet. 2003. PMID: 12960210 Free PMC article.
76 results