These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

79 related items for PubMed ID: 9215754

  • 1. HLA-H mutations in the Ashkenazi Jewish population.
    Beutler E, Gelbart T.
    Blood Cells Mol Dis; 1997; 23(1):95-8. PubMed ID: 9215754
    [Abstract] [Full Text] [Related]

  • 2. Frequencies of C282Y and H63D alleles in the HFE gene among various Jewish ethnic groups in Israel: a change of concept required.
    Reish O, Shefer-Kaufmann N, Shimshoni DC, Renbaum P, Orr-Urtreger A, Steiner H, Rapoport M, Levy-Lahad E, Altarescu G.
    Genet Med; 2010 Feb; 12(2):122-5. PubMed ID: 20084012
    [Abstract] [Full Text] [Related]

  • 3. Celtic origin of the C282Y mutation of hemochromatosis.
    Lucotte G.
    Blood Cells Mol Dis; 1998 Dec; 24(4):433-8. PubMed ID: 9851897
    [Abstract] [Full Text] [Related]

  • 4. Frequency analysis and allele map in favor of the celtic origin of the C282Y mutation of hemochromatosis.
    Lucotte G.
    Blood Cells Mol Dis; 2001 Dec; 27(2):549-56. PubMed ID: 11500066
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Frequency of the C282Y mutation of hemochromatosis in five French populations.
    Mercier G, Bathelier C, Lucotte G.
    Blood Cells Mol Dis; 1998 Jun; 24(2):165-6. PubMed ID: 9642097
    [Abstract] [Full Text] [Related]

  • 9. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL, Ou CY, Cappuccio J, Braggins C, Dunnigan K, Phatak PD.
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
    [Abstract] [Full Text] [Related]

  • 10. A population-based study of the clinical expression of the hemochromatosis gene.
    Olynyk JK, Cullen DJ, Aquilia S, Rossi E, Summerville L, Powell LW.
    N Engl J Med; 1999 Sep 02; 341(10):718-24. PubMed ID: 10471457
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern England.
    Willis G, Jennings BA, Goodman E, Fellows IW, Wimperis JZ.
    Blood Cells Mol Dis; 1997 Aug 02; 23(2):288-91. PubMed ID: 9410472
    [Abstract] [Full Text] [Related]

  • 13. HLA-H and associated proteins in patients with hemochromatosis.
    Beutler E, West C, Gelbart T.
    Mol Med; 1997 Jun 02; 3(6):397-402. PubMed ID: 9234244
    [Abstract] [Full Text] [Related]

  • 14. Mutation analysis of the HFE gene in Brazilian populations.
    Agostinho MF, Arruda VR, Basseres DS, Bordin S, Soares MC, Menezes RC, Costa FF, Saad ST.
    Blood Cells Mol Dis; 1999 Jun 02; 25(5-6):324-7. PubMed ID: 10660479
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. [The usefulness of the detection of Cys282Tyr and His63Asp mutations in the diagnosis of hereditary hemochromatosis].
    Moreno L, Vallcorba P, Boixeda D, Cabello P, Bermejo F, San Román C.
    Rev Clin Esp; 1999 Oct 02; 199(10):632-6. PubMed ID: 10589245
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. 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 02; 14(3):251-2. PubMed ID: 8896550
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 4.