Bomford AB - Search Results

1

Sebastiani G, Wallace DF, Lioumi M, Goutos I, Mitchell WA, Bomford AB, Dhillon AP, Dooley JS, Ragoussis J, Walker AP. Sebastiani G, et al. Among authors: bomford ab. J Hepatol. 2003 Mar;38(3):376-7. doi: 10.1016/s0168-8278(02)00426-9. J Hepatol. 2003. PMID: 12586309 No abstract available.

2

Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y.

Wallace DF, Walker AP, Pietrangelo A, Clare M, Bomford AB, Dixon JL, Powell LW, Subramaniam VN, Dooley JS. Wallace DF, et al. Among authors: bomford ab. J Hepatol. 2002 Apr;36(4):474-9. doi: 10.1016/s0168-8278(01)00304-x. J Hepatol. 2002. PMID: 11943417

3

Haemochromatosis: a gene at last?

Robson KJ, Shearman JD, Merryweather-Clarke AT, Pointon JJ, Rosenberg WM, Walker AP, Dooley JS, Bomford A, Raha-Chowdhury R, Worwood M. Robson KJ, et al. J Med Genet. 1997 Feb;34(2):148-51. doi: 10.1136/jmg.34.2.148. J Med Genet. 1997. PMID: 9039993 Free PMC article. No abstract available.

4

A 6p22 reference map of leukocyte DNA: exclusion of rearrangement in four cases of atypical haemochromatosis.

Wallace DF, Partridge J, Robertson A, Simpson VM, Worwood M, Bomford AB, Volz A, Ziegler A, Dooley JS, Walker AP. Wallace DF, et al. Among authors: bomford ab. Eur J Hum Genet. 1998 Sep-Oct;6(5):523-6. doi: 10.1038/sj.ejhg.5200216. Eur J Hum Genet. 1998. PMID: 9801878

5

Atypical haemochromatosis: phenotypic spectrum and beta2-microglobulin candidate gene analysis.

Walker AP, Wallace DF, Partridge J, Bomford AB, Dooley JS. Walker AP, et al. Among authors: bomford ab. J Med Genet. 1999 Jul;36(7):537-41. J Med Genet. 1999. PMID: 10424814 Free PMC article.

6

Hemochromatosis-related mutation detection.

Merryweather-Clarke AT, Shearman JD, Robson KJ, Pointon JJ, Liu YT, Bomford A, Dooley J, Walker AP, Worwood M. Merryweather-Clarke AT, et al. Blood. 1998 Apr 1;91(7):2620-1. Blood. 1998. PMID: 9516166 Free article. No abstract available.

7

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium.

Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJ, Jouanolle AM, Mosser A, David V, Le Gall JY, Halsall DJ, Elsey TS, Kelly A, Cox TM, Clare M, Bomford A, Vandwalle JL, Rochette J, Borot N, Coppin H, Roth MP, Ryan E, Crowe J, Totaro A, Gasparini P, Roetto A, Walker AP, et al. Merryweather-Clarke AT, et al. Nat Genet. 1999 Nov;23(3):271. doi: 10.1038/15452. Nat Genet. 1999. PMID: 10545942 No abstract available.

8

Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis.

Datz C, Lalloz MR, Vogel W, Graziadei I, Hackl F, Vautier G, Layton DM, Maier-Dobersberger T, Ferenci P, Penner E, Sandhofer F, Bomford A, Paulweber B. Datz C, et al. J Hepatol. 1997 Nov;27(5):773-9. doi: 10.1016/s0168-8278(97)80312-1. J Hepatol. 1997. PMID: 9382962

9

Haemochromatosis.

Bomford A. Bomford A. J R Soc Med. 1979 May;72(5):311-4. doi: 10.1177/014107687907200501. J R Soc Med. 1979. PMID: 552522 Free PMC article. No abstract available.

10

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.

Merryweather-Clarke AT, Cadet E, Bomford A, Capron D, Viprakasit V, Miller A, McHugh PJ, Chapman RW, Pointon JJ, Wimhurst VL, Livesey KJ, Tanphaichitr V, Rochette J, Robson KJ. Merryweather-Clarke AT, et al. Hum Mol Genet. 2003 Sep 1;12(17):2241-7. doi: 10.1093/hmg/ddg225. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915468

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