Thakker RV - Search Results

1

An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism.

Bowl MR, Nesbit MA, Harding B, Levy E, Jefferson A, Volpi E, Rizzoti K, Lovell-Badge R, Schlessinger D, Whyte MP, Thakker RV. Bowl MR, et al. Among authors: thakker rv. J Clin Invest. 2005 Oct;115(10):2822-31. doi: 10.1172/JCI24156. Epub 2005 Sep 15. J Clin Invest. 2005. PMID: 16167084 Free PMC article.

2

Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies.

Thakker RV, Davies KE, Whyte MP, Wooding C, O'Riordan JL. Thakker RV, et al. J Clin Invest. 1990 Jul;86(1):40-5. doi: 10.1172/JCI114712. J Clin Invest. 1990. PMID: 1973175 Free PMC article.

3

Bridging markers defining the map position of X linked hypophosphataemic rickets.

Thakker RV, Read AP, Davies KE, Whyte MP, Weksberg R, Glorieux F, Davies M, Mountford RC, Harris R, King A, et al. Thakker RV, et al. J Med Genet. 1987 Dec;24(12):756-60. doi: 10.1136/jmg.24.12.756. J Med Genet. 1987. PMID: 2828625 Free PMC article.

4

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: thakker rv. Hum Genet. 1995 Aug;96(2):183-7. doi: 10.1007/BF00207376. Hum Genet. 1995. PMID: 7635467

5

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: thakker rv. J Clin Invest. 1993 Jun;91(6):2351-7. doi: 10.1172/JCI116467. J Clin Invest. 1993. PMID: 8099916 Free PMC article.

6

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. Ann Hum Genet. 1993 Jan;57(1):17-25. doi: 10.1111/j.1469-1809.1993.tb00883.x. Ann Hum Genet. 1993. PMID: 8101435

7

Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations.

Thakker RV, Pook MA, Wooding C, Boscaro M, Scanarini M, Clayton RN. Thakker RV, et al. J Clin Invest. 1993 Jun;91(6):2815-21. doi: 10.1172/JCI116524. J Clin Invest. 1993. PMID: 8514889 Free PMC article.

8

Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1.

Trump D, Pilia G, Dixon PH, Wooding C, Thakrar R, Leigh SE, Nagaraja R, Whyte MP, Schlessinger D, Thakker RV. Trump D, et al. Among authors: thakker rv. Hum Genet. 1996 Jan;97(1):60-8. doi: 10.1007/BF00218834. Hum Genet. 1996. PMID: 8557262

9

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. Among authors: thakker rv. Hum Genet. 1996 Jun;97(6):732-41. doi: 10.1007/BF02346182. Hum Genet. 1996. PMID: 8641689

10

EagI and NotI linking clones from human chromosomes 11 and Xp.

Pook MA, Thakrar R, Pottinger B, Harding B, Porteous D, van Heyningen V, Cowell J, Jones C, Povey S, Davies KE, Thakker RV. Pook MA, et al. Among authors: thakker rv. Hum Genet. 1996 Jun;97(6):742-9. doi: 10.1007/BF02346183. Hum Genet. 1996. PMID: 8641690

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