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181 related items for PubMed ID: 9032645

  • 1. 46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosis.
    Venditti CP, Seese NK, Gerhard GS, Ten Elshof AE, Chorney KA, Mowrey PN, Lacey PG, Knoll JH, Chorney MJ.
    J Med Genet; 1997 Jan; 34(1):24-7. PubMed ID: 9032645
    [Abstract] [Full Text] [Related]

  • 2. Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE).
    Gandon G, Jouanolle AM, Chauvel B, Mauvieux V, le Treut A, Feingold J, Le Gall JY, David V, Yaouanq J.
    Hum Genet; 1996 Jan; 97(1):103-13. PubMed ID: 8557248
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  • 3. Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F.
    Gasparini P, Borgato L, Piperno A, Girelli D, Olivieri O, Gottardi E, Roetto A, Dianzani I, Fargion S, Schinaia G.
    Hum Mol Genet; 1993 May; 2(5):571-6. PubMed ID: 8518796
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  • 4. Characterization of a recombinant that locates the hereditary hemochromatosis gene telomeric to HLA-F.
    Calandro LM, Baer DM, Sensabaugh GF.
    Hum Genet; 1995 Sep; 96(3):339-42. PubMed ID: 7649553
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  • 5. Linkage to chromosome 1q in Greek families with juvenile hemochromatosis.
    Papanikolaou G, Politou M, Roetto A, Bosio S, Sakelaropoulos N, Camaschella C, Loukopoulos D.
    Blood Cells Mol Dis; 2001 Sep; 27(4):744-9. PubMed ID: 11778658
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  • 6. Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE).
    Yaouanq J, Perichon M, Chorney M, Pontarotti P, Le Treut A, el Kahloun A, Mauvieux V, Blayau M, Jouanolle AM, Chauvel B.
    Am J Hum Genet; 1994 Feb; 54(2):252-63. PubMed ID: 8304342
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  • 7. Recombinations defining centromeric and telomeric borders for the hereditary haemochromatosis locus.
    Ajioka RS, Yu P, Gruen JR, Edwards CQ, Griffen LM, Kushner JP.
    J Med Genet; 1997 Jan; 34(1):28-33. PubMed ID: 9032646
    [Abstract] [Full Text] [Related]

  • 8. Clone-contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22.
    Lauer P, Meyer NC, Prass CE, Starnes SM, Wolff RK, Gnirke A.
    Genome Res; 1997 May; 7(5):457-70. PubMed ID: 9149942
    [Abstract] [Full Text] [Related]

  • 9. Haemochromatosis in patients with beta-thalassaemia trait.
    Piperno A, Mariani R, Arosio C, Vergani A, Bosio S, Fargion S, Sampietro M, Girelli D, Fraquelli M, Conte D, Fiorelli G, Camaschella C.
    Br J Haematol; 2000 Dec; 111(3):908-14. PubMed ID: 11122155
    [Abstract] [Full Text] [Related]

  • 10. Detection of hereditary haemochromatosis in an HLA-identical pedigree showing discordance between HLA class I genes and the disease locus.
    Dokal I, Lord D, Rhodes D, Bydder G, Cox T.
    Hum Genet; 1991 Dec; 88(2):209-14. PubMed ID: 1757096
    [Abstract] [Full Text] [Related]

  • 11. New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105.
    Raha-Chowdhury R, Bowen DJ, Stone C, Pointon JJ, Terwilliger JD, Shearman JD, Robson KJ, Bomford A, Worwood M.
    Hum Mol Genet; 1995 Oct; 4(10):1869-74. PubMed ID: 8595409
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  • 13. The haemochromatosis candidate gene HFE (HLA-H) of man and mouse is located in syntenic regions within the histone gene cluster.
    Albig W, Drabent B, Burmester N, Bode C, Doenecke D.
    J Cell Biochem; 1998 May 01; 69(2):117-26. PubMed ID: 9548560
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  • 14. A recombination event close to HFE gene in hereditary hemochromatosis.
    Roetto A, Sbaiz L, Bosio S, Piperno A, Fargion S, Carella M, Totaro A, Grifa A, Gasparini P, Camaschella C.
    Ann Genet; 1997 May 01; 40(3):150-3. PubMed ID: 9401103
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  • 15. A PCR-SSP method for detecting the His63Asp mutation in the HFE gene associated with hereditary haemochromatosis.
    Smillie D.
    Mol Pathol; 1998 Aug 01; 51(4):232-3. PubMed ID: 9893753
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