Thakker RV - Search Results

1

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.

2

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. Among authors: thakker rv. Henry Ford Hosp Med J. 1992;40(3-4):162-6. Henry Ford Hosp Med J. 1992. PMID: 1362397 Free article.

3

Determination of a molecular map position for Hyp using a new interspecific backcross produced by in vitro fertilization.

Kay G, Thakker RV, Rastan S. Kay G, et al. Among authors: thakker rv. Genomics. 1991 Nov;11(3):651-7. doi: 10.1016/0888-7543(91)90072-m. Genomics. 1991. PMID: 1685478

4

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.

5

Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families.

Thakker RV, Davies KE, Read AP, Tippett P, Wooding C, Flint T, Wood S, Kruse TA, Whyte MP, O'Riordan JL. Thakker RV, et al. Genomics. 1990 Oct;8(2):189-93. doi: 10.1016/0888-7543(90)90271-u. Genomics. 1990. PMID: 1979046

6

Gene mapping of mineral metabolic disorders.

Thakker RV, Davies KE, O'Riordan JL. Thakker RV, et al. J Inherit Metab Dis. 1989;12 Suppl 1:231-46. doi: 10.1007/BF01799298. J Inherit Metab Dis. 1989. PMID: 2681997 Review.

7

Molecular analysis of X-linked diseases.

Davies KE, Ball SP, Dorkins HR, Forrest SM, Kenwrick SJ, Patterson MN, Smith TJ, Old JM, King AW, Thakker RV, et al. Davies KE, et al. Among authors: thakker rv. Ann Clin Res. 1986;18(5-6):231-3. Ann Clin Res. 1986. PMID: 2882726 No abstract available.

8

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis.

Read AP, Thakker RV, Davies KE, Mountford RC, Brenton DP, Davies M, Glorieux F, Harris R, Hendy GN, King A, et al. Read AP, et al. Among authors: thakker rv. Hum Genet. 1986 Jul;73(3):267-70. doi: 10.1007/BF00401242. Hum Genet. 1986. PMID: 3015770

9

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

10

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.

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