BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 7847378)

  • 1. Haplotype analysis in Australian hemochromatosis patients: evidence for a predominant ancestral haplotype exclusively associated with hemochromatosis.
    Jazwinska EC; Pyper WR; Burt MJ; Francis JL; Goldwurm S; Webb SI; Lee SC; Halliday JW; Powell LW
    Am J Hum Genet; 1995 Feb; 56(2):428-33. PubMed ID: 7847378
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Allelic association of microsatellites of 6p in Italian hemochromatosis patients.
    Camaschella C; Roetto A; Gasparini P; Piperno A; Fortina P; Surrey S; Rappaport E
    Hum Genet; 1996 Apr; 97(4):476-81. PubMed ID: 8834246
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Allelic associations and homozygosity at loci from HLA-B to D6S299 in genetic haemochromatosis.
    Raha-Chowdhury R; Bowen DJ; Burnett AK; Worwood M
    J Med Genet; 1995 Jun; 32(6):446-52. PubMed ID: 7666396
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Localization of the hemochromatosis gene close to D6S105.
    Jazwinska EC; Lee SC; Webb SI; Halliday JW; Powell LW
    Am J Hum Genet; 1993 Aug; 53(2):347-52. PubMed ID: 8328453
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage disequilibrium analysis in Australian haemochromatosis patients indicates bipartite association with clinical expression.
    Pratiwi R; Fletcher LM; Pyper WR; Do KA; Crawford DH; Powell LW; Jazwinska EC
    J Hepatol; 1999 Jul; 31(1):39-46. PubMed ID: 10424281
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes.
    Ajioka RS; Jorde LB; Gruen JR; Yu P; Dimitrova D; Barrow J; Radisky E; Edwards CQ; Griffen LM; Kushner JP
    Am J Hum Genet; 1997 Jun; 60(6):1439-47. PubMed ID: 9199565
    [TBL] [Abstract][Full Text] [Related]  

  • 10. HLA haplotype map of river valley populations with hemochromatosis traced through five centuries in Central Sweden.
    Olsson KS; Ritter B; Hansson N; Chowdhury RR
    Eur J Haematol; 2008 Jul; 81(1):36-46. PubMed ID: 18363869
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the gene.
    Crawford DH; Powell LW; Leggett BA; Francis JS; Fletcher LM; Webb SI; Halliday JW; Jazwinska EC
    Am J Hum Genet; 1995 Aug; 57(2):362-7. PubMed ID: 7668262
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A haplotype and linkage disequilibrium analysis of the hereditary hemochromatosis gene region.
    Thomas W; Fullan A; Loeb DB; McClelland EE; Bacon BR; Wolff RK
    Hum Genet; 1998 May; 102(5):517-25. PubMed ID: 9654199
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? HLA haplotype observations of hemochromatosis from the west coast of Sweden.
    Olsson KS; Konar J; Dufva IH; Ricksten A; Raha-Chowdhury R
    Eur J Haematol; 2011 Jan; 86(1):75-82. PubMed ID: 20946107
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients.
    Piperno A; Arosio C; Fargion S; Roetto A; Nicoli C; Girelli D; Sbaiz L; Gasparini P; Boari G; Sampietro M; Camaschella C
    Hepatology; 1996 Jul; 24(1):43-6. PubMed ID: 8707280
    [TBL] [Abstract][Full Text] [Related]  

  • 15. HLA-A3-B14 and the origin of the haemochromatosis C282Y mutation: founder effects and recombination events during 12 generations in a Scandinavian family with major iron overload.
    Olsson KS; Ritter B; Raha-Chowdhury R
    Eur J Haematol; 2010 Feb; 84(2):145-53. PubMed ID: 19912313
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload.
    Cruz E; Vieira J; Almeida S; Lacerda R; Gartner A; Cardoso CS; Alves H; Porto G
    BMC Med Genet; 2006 Mar; 7():16. PubMed ID: 16509978
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 27(4):744-9. PubMed ID: 11778658
    [TBL] [Abstract][Full Text] [Related]  

  • 18. HLA determinants in an Australian population of hemochromatosis patients and their families.
    Summers KM; Tam KS; Halliday JW; Powell LW
    Am J Hum Genet; 1989 Jul; 45(1):41-8. PubMed ID: 2741950
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Isolation of CA dinucleotide repeats close to D6S105; linkage disequilibrium with haemochromatosis.
    Stone C; Pointon JJ; Jazwinska EC; Halliday JW; Powell LW; Robson KJ; Monaco AP; Weatherall DJ
    Hum Mol Genet; 1994 Nov; 3(11):2043-6. PubMed ID: 7874124
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.