Thakker RV - Search Results

1

Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda.

Christie PT, Curley A, Nesbit MA, Chapman C, Genet S, Harper PS, Keeling SL, Wilkie AO, Winter RM, Thakker RV. Christie PT, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 2001 Jul;86(7):3233-6. doi: 10.1210/jcem.86.7.7688. J Clin Endocrinol Metab. 2001. PMID: 11443194

2

Genetic linkage studies of X-linked hypophosphataemic rickets in a Saudi Arabian family.

Thakker RV, Farmery MR, Sakati NA, Milner RD. Thakker RV, et al. Clin Endocrinol (Oxf). 1992 Oct;37(4):338-43. doi: 10.1111/j.1365-2265.1992.tb02335.x. Clin Endocrinol (Oxf). 1992. PMID: 1483289

3

The role of molecular genetics in screening for multiple endocrine neoplasia type 1.

Thakker RV. Thakker RV. Endocrinol Metab Clin North Am. 1994 Mar;23(1):117-35. Endocrinol Metab Clin North Am. 1994. PMID: 7913020 Review.

4

The molecular genetics of the multiple endocrine neoplasia syndromes.

Thakker RV. Thakker RV. Clin Endocrinol (Oxf). 1993 Jan;38(1):1-14. doi: 10.1111/j.1365-2265.1993.tb00964.x. Clin Endocrinol (Oxf). 1993. PMID: 8094647 Review. No abstract available.

5

Molecular genetic studies of sporadic pituitary tumors.

Boggild MD, Jenkinson S, Pistorello M, Boscaro M, Scanarini M, McTernan P, Perrett CW, Thakker RV, Clayton RN. Boggild MD, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 1994 Feb;78(2):387-92. doi: 10.1210/jcem.78.2.8106627. J Clin Endocrinol Metab. 1994. PMID: 8106627

6

Association of familial Duane anomaly and urogenital abnormalities with a bisatellited marker derived from chromosome 22.

Cullen P, Rodgers CS, Callen DF, Connolly VM, Eyre H, Fells P, Gordon H, Winter RM, Thakker RV. Cullen P, et al. Among authors: thakker rv. Am J Med Genet. 1993 Nov 1;47(6):925-30. doi: 10.1002/ajmg.1320470623. Am J Med Genet. 1993. PMID: 8279492

7

Allelic deletion in pituitary adenomas reflects aggressive biological activity and has potential value as a prognostic marker.

Bates AS, Farrell WE, Bicknell EJ, McNicol AM, Talbot AJ, Broome JC, Perrett CW, Thakker RV, Clayton RN. Bates AS, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 1997 Mar;82(3):818-24. doi: 10.1210/jcem.82.3.3799. J Clin Endocrinol Metab. 1997. PMID: 9062489

8

Characterization of mutations in patients with multiple endocrine neoplasia type 1.

Bassett JH, Forbes SA, Pannett AA, Lloyd SE, Christie PT, Wooding C, Harding B, Besser GM, Edwards CR, Monson JP, Sampson J, Wass JA, Wheeler MH, Thakker RV. Bassett JH, et al. Among authors: thakker rv. Am J Hum Genet. 1998 Feb;62(2):232-44. doi: 10.1086/301729. Am J Hum Genet. 1998. PMID: 9463336 Free PMC article.

9

Mutational analysis of PHEX gene in X-linked hypophosphatemia.

Dixon PH, Christie PT, Wooding C, Trump D, Grieff M, Holm I, Gertner JM, Schmidtke J, Shah B, Shaw N, Smith C, Tau C, Schlessinger D, Whyte MP, Thakker RV. Dixon PH, et al. Among authors: thakker rv. J Clin Endocrinol Metab. 1998 Oct;83(10):3615-23. doi: 10.1210/jcem.83.10.5180. J Clin Endocrinol Metab. 1998. PMID: 9768674

10

GNAS1 mutational analysis in pseudohypoparathyroidism.

Ahmed SF, Dixon PH, Bonthron DT, Stirling HF, Barr DG, Kelnar CJ, Thakker RV. Ahmed SF, et al. Among authors: thakker rv. Clin Endocrinol (Oxf). 1998 Oct;49(4):525-31. Clin Endocrinol (Oxf). 1998. PMID: 9876352

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