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Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
Teh BT, 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, et al. Among authors: delbridge lw. Hum Genet. 2004 Jan;114(2):223. doi: 10.1007/s00439-003-1060-z. Hum Genet. 2004. PMID: 15046102 No abstract available.
Fine-structure deletion mapping of 10q22-24 identifies regions of loss of heterozygosity and suggests that sporadic follicular thyroid adenomas and follicular thyroid carcinomas develop along distinct neoplastic pathways.
Yeh JJ, Marsh DJ, Zedenius J, Dwight T, Delbridge L, Robinson BG, Eng C. Yeh JJ, et al. Genes Chromosomes Cancer. 1999 Dec;26(4):322-8. doi: 10.1002/(sici)1098-2264(199912)26:4<322::aid-gcc6>3.0.co;2-#. Genes Chromosomes Cancer. 1999. PMID: 10534767
Minimally invasive parathyroidectomy: 50 consecutive cases.
Delbridge LW, Dolan SJ, Hop TT, Robinson BG, Wilkinson MR, Reeve TS. Delbridge LW, et al. Med J Aust. 2000 May 1;172(9):418-22. doi: 10.5694/j.1326-5377.2000.tb124036.x. Med J Aust. 2000. PMID: 10870533 Clinical Trial.
310 results