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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: nelson ae. Hum Genet. 2004 Jan;114(2):222. doi: 10.1007/s00439-003-1060-z. Hum Genet. 2004. PMID: 15046094 No abstract available.
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. Among authors: nelson ae. 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.
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: nelson ae. Hum Genet. 2004 Jan;114(2):221. doi: 10.1007/s00439-003-1060-z. Hum Genet. 2004. PMID: 15046050 No abstract available.
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: nelson ae. Hum Genet. 2004 Jan;114(2):222. doi: 10.1007/s00439-003-1060-z. Hum Genet. 2004. PMID: 15046098 No abstract available.
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: nelson ae. Hum Genet. 2004 Jan;114(2):223. doi: 10.1007/s00439-003-1060-z. Hum Genet. 2004. PMID: 15046102 No abstract available.
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: nelson ae. Hum Genet. 2004 Jan;114(2):223. doi: 10.1007/s00439-003-1060-z. Hum Genet. 2004. PMID: 15046105 No abstract available.
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: nelson ae. Hum Genet. 2004 Jan;114(2):223. doi: 10.1007/s00439-003-1060-z. Hum Genet. 2004. PMID: 15046107 No abstract available.
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: nelson ae. Hum Genet. 2004 Jan;114(2):224. doi: 10.1007/s00439-003-1060-z. Hum Genet. 2004. PMID: 15046109 No abstract available.
Gene expression of parathyroid tumors: molecular subclassification and identification of the potential malignant phenotype.
Haven CJ, Howell VM, Eilers PH, Dunne R, Takahashi M, van Puijenbroek M, Furge K, Kievit J, Tan MH, Fleuren GJ, Robinson BG, Delbridge LW, Philips J, Nelson AE, Krause U, Dralle H, Hoang-Vu C, Gimm O, Morreau H, Marsh DJ, Teh BT. Haven CJ, et al. Among authors: nelson ae. Cancer Res. 2004 Oct 15;64(20):7405-11. doi: 10.1158/0008-5472.CAN-04-2063. Cancer Res. 2004. PMID: 15492263
214 results