290 related articles for article (PubMed ID: 8896549)
1. Haemochromatosis and HLA-H.
Jazwinska EC; Cullen LM; Busfield F; Pyper WR; Webb SI; Powell LW; Morris CP; Walsh TP
Nat Genet; 1996 Nov; 14(3):249-51. PubMed ID: 8896549
[No Abstract] [Full Text] [Related]
2. Haemochromatosis and HLA-H.
Jouanolle AM; Gandon G; Jézéquel P; Blayau M; Campion ML; Yaouanq J; Mosser J; Fergelot P; Chauvel B; Bouric P; Carn G; Andrieux N; Gicquel I; Le Gall JY; David V
Nat Genet; 1996 Nov; 14(3):251-2. PubMed ID: 8896550
[No Abstract] [Full Text] [Related]
3. Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis.
Jeffrey GP; Chakrabarti S; Hegele RA; Adams PC
Nat Genet; 1999 Aug; 22(4):325-6. PubMed ID: 10431233
[No Abstract] [Full Text] [Related]
4. Genetic irony beyond haemochromatosis: clinical effects of HLA-H mutations.
Beutler E
Lancet; 1997 Feb; 349(9048):296-7. PubMed ID: 9024367
[No Abstract] [Full Text] [Related]
5. Haemochromatosis: strike while the iron is hot.
Cox T
Nat Genet; 1996 Aug; 13(4):386-8. PubMed ID: 8696327
[No Abstract] [Full Text] [Related]
6. Haemochromatosis, HFE and genetic complexity.
Risch N
Nat Genet; 1997 Dec; 17(4):375-6. PubMed ID: 9398831
[No Abstract] [Full Text] [Related]
7. Clinical implications of the hemochromatosis gene.
Tavill AS
N Engl J Med; 1999 Sep; 341(10):755-7. PubMed ID: 10471465
[No Abstract] [Full Text] [Related]
8. [Genetic background and DNA diagnostics of hemochromatosis].
Heliö T; Färkkilä M; Halme L; Karlsson M; Palotie A; Kontula K
Duodecim; 1998; 114(14):1404-9. PubMed ID: 11552248
[No Abstract] [Full Text] [Related]
9. Haemochromatosis gene C282Y homozygotes in an elderly male population.
Willis G; Wimperis JZ; Smith KC; Fellows IW; Jennings BA
Lancet; 1999 Jul; 354(9174):221-2. PubMed ID: 10421310
[TBL] [Abstract][Full Text] [Related]
10. Haemochromatosis... definite maybe!
Nat Genet; 1996 Aug; 13(4):375-6. PubMed ID: 8696321
[No Abstract] [Full Text] [Related]
11. High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation.
Tordai A; Andrikovics H; Kalmár L; Rajczy K; Pénzes M; Sarkadi B; Klein I; Váradi A
J Med Genet; 1998 Oct; 35(10):878-9. PubMed ID: 9783719
[No Abstract] [Full Text] [Related]
12. Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis.
de Villiers JN; Scholtz CL; Hoogendijk CF; Cawood EJ; Kotze MJ
Hum Genet; 1998 Jan; 102(1):127. PubMed ID: 9490291
[No Abstract] [Full Text] [Related]
13. Haemochromatosis case detection by genetic testing: a new era.
Kilpatrick ES; Jagger C
Ann Clin Biochem; 1998 Sep; 35 ( Pt 5)():674-7. PubMed ID: 9768336
[No Abstract] [Full Text] [Related]
14. Haemochromatosis mutation analysis in a normal Irish population.
Ryan F; Vaughan J
Br J Biomed Sci; 2000; 57(4):315-6. PubMed ID: 11204863
[No Abstract] [Full Text] [Related]
15. [Hereditary hemochromatosis].
Parkkila S
Duodecim; 2000; 116(8):829-36. PubMed ID: 11787126
[No Abstract] [Full Text] [Related]
16. Putting a hold on 'HLA-H'.
Mercier B; Mura C; Ferec C
Nat Genet; 1997 Mar; 15(3):234. PubMed ID: 9054932
[No Abstract] [Full Text] [Related]
17. Overestimation of HFE C282Y homozygous hemochromatosis prevalence as the result of a common primer-binding site polymorphism.
Press RD
Mol Diagn; 1999 Dec; 4(4):391-2. PubMed ID: 10671650
[No Abstract] [Full Text] [Related]
18. 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
Nat Genet; 1999 Nov; 23(3):271. PubMed ID: 10545942
[No Abstract] [Full Text] [Related]
19. The discovery of HFE.
Bacon BR
Curr Gastroenterol Rep; 1999; 1(1):7. PubMed ID: 10980918
[No Abstract] [Full Text] [Related]
20. 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
J Hepatol; 1997 Nov; 27(5):773-9. PubMed ID: 9382962
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]