Pang JT - Search Results

1

Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH.

Trump D, Whyte MP, Wooding C, Pang JT, Pearce SH, Kocher DB, Thakker RV. Trump D, et al. Among authors: pang jt. Hum Genet. 1995 Aug;96(2):183-7. doi: 10.1007/BF00207376. Hum Genet. 1995. PMID: 7635467

2

Linkage analysis of 7 polymorphic markers at chromosome 11p11.2-11q13 in 27 multiple endocrine neoplasia type 1 families.

Thakker RV, Wooding C, Pang JT, Farren B, Harding B, Anderson DC, Besser GM, Bouloux P, Brenton DP, Buchanan KD. Thakker RV, et al. Among authors: pang jt. Ann Hum Genet. 1993 Jan;57(1):17-25. doi: 10.1111/j.1469-1809.1993.tb00883.x. Ann Hum Genet. 1993. PMID: 8101435

3

Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene.

Pang JT, Lloyd SE, Wooding C, Farren B, Pottinger B, Harding B, Leigh SE, Pook MA, Benham FJ, Gillett GT, Taggart RT, Thakker RV. Pang JT, et al. Hum Genet. 1996 Jun;97(6):732-41. doi: 10.1007/BF02346182. Hum Genet. 1996. PMID: 8641689

4

Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).

Lloyd SE, Pang JT, Pearce SH, Leigh SE, Thakker RV. Lloyd SE, et al. Among authors: pang jt. Hum Genet. 1997 May;99(5):585-9. doi: 10.1007/s004390050410. Hum Genet. 1997. PMID: 9150722

5

Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneity.

Gertner JM, Whyte MP, Dixon PH, Pang JT, Trump D, Pearce SH, Wooding C, Thakker RV. Gertner JM, et al. Among authors: pang jt. J Bone Miner Res. 1997 Aug;12(8):1204-9. doi: 10.1359/jbmr.1997.12.8.1204. J Bone Miner Res. 1997. PMID: 9258750 Free article.

6

Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36.

Williamson C, Pannett AA, Pang JT, Wooding C, McCarthy M, Sheppard MN, Monson J, Clayton RN, Thakker RV. Williamson C, et al. Among authors: pang jt. J Med Genet. 1997 Aug;34(8):617-9. doi: 10.1136/jmg.34.8.617. J Med Genet. 1997. PMID: 9279750 Free PMC article.

7

Molecular genetic mapping of the multiple endocrine neoplasia type 1 locus.

Pang JT, Pook MA, Eubanks JH, Jones C, van Heyningen V, Evans GA, Thakker RV. Pang JT, et al. Henry Ford Hosp Med J. 1992;40(3-4):162-6. Henry Ford Hosp Med J. 1992. PMID: 1362397 Free article.

8

Multiple endocrine neoplasia type 1 (MEN1).

Pang JT, Thakker RV. Pang JT, et al. Eur J Cancer. 1994;30A(13):1961-8. doi: 10.1016/0959-8049(94)00387-k. Eur J Cancer. 1994. PMID: 7734208 Review. No abstract available.

9

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.

Scheinman SJ, Pook MA, Wooding C, Pang JT, Frymoyer PA, Thakker RV. Scheinman SJ, et al. Among authors: pang jt. J Clin Invest. 1993 Jun;91(6):2351-7. doi: 10.1172/JCI116467. J Clin Invest. 1993. PMID: 8099916 Free PMC article.

10

Clinical studies of multiple endocrine neoplasia type 1 (MEN1).

Trump D, Farren B, Wooding C, Pang JT, Besser GM, Buchanan KD, Edwards CR, Heath DA, Jackson CE, Jansen S, Lips K, Monson JP, O'Halloran D, Sampson J, Shalet SM, Wheeler MH, Zink A, Thakker RV. Trump D, et al. Among authors: pang jt. QJM. 1996 Sep;89(9):653-69. doi: 10.1093/qjmed/89.9.653. QJM. 1996. PMID: 8917740

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