153 related articles for article (PubMed ID: 6578890)
1. An HLA-All association with the hemochromatosis allele?
Le Mignon L; Simon M; Fauchet R; Edan G; Le Reun M; Brissot P; Genetet B; Bourel M
Clin Genet; 1983 Sep; 24(3):171-6. PubMed ID: 6578890
[TBL] [Abstract][Full Text] [Related]
2. A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA association.
Simon M; Le Mignon L; Fauchet R; Yaouanq J; David V; Edan G; Bourel M
Am J Hum Genet; 1987 Aug; 41(2):89-105. PubMed ID: 3475981
[TBL] [Abstract][Full Text] [Related]
3. Idiopathic haemochromatosis and HLA antigens in Italy: is A3 Bw35 HLA haplotype a marker for idiopathic haemochromatosis gene in north east regions?
Piperno A; Fargion S; Panaiotopoulos N; Del Ninno E; Taddei MT; Fiorelli G
J Clin Pathol; 1986 Feb; 39(2):125-8. PubMed ID: 3485115
[TBL] [Abstract][Full Text] [Related]
4. Is all genetic (hereditary) hemochromatosis HLA-associated.
Powell LW; Bassett ML; Axelsen E; Ferluga J; Halliday JW
Ann N Y Acad Sci; 1988; 526():23-33. PubMed ID: 3260461
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Immunogenetic markers of the HLA system in idiopathic hemochromatosis. Contribution and value].
Fauchet R; Simon M
Presse Med; 1984 May; 13(21):1307-9. PubMed ID: 6233551
[No Abstract] [Full Text] [Related]
7. Co-selection of the H63D mutation and the HLA-A29 allele: a new paradigm of linkage disequilibrium?
Cardoso CS; Alves H; Mascarenhas M; Gonçalves R; Oliveira P; Rodrigues P; Cruz E; de Sousa M; Porto G
Immunogenetics; 2002 Mar; 53(12):1002-8. PubMed ID: 11904676
[TBL] [Abstract][Full Text] [Related]
8. Disease risk estimates from marker association data. Application to individuals at risk for hemochromatosis.
Lin HJ; Conte WJ; Rotter JI
Clin Genet; 1985 Feb; 27(2):127-33. PubMed ID: 3856493
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. HLA determinants in idiopathic hemochromatosis.
Fauchet R; Genetet N; Genetet B; Simon M; Bourel M
Tissue Antigens; 1979 Jul; 14(1):10-4. PubMed ID: 91216
[TBL] [Abstract][Full Text] [Related]
11. Idiopathic hemochromatosis: significance and implications of linkage and association to HLA.
Lalouel JM; Jorde LB
Ann N Y Acad Sci; 1988; 526():34-46. PubMed ID: 3291686
[No Abstract] [Full Text] [Related]
12. [Idiopathic hemochromatosis. Immunogenetics and diagnosis. Prevention by HLA genotypes].
Fauchet R; Lemignon L; Bourel M; Genetet B; Simon M
Pathol Biol (Paris); 1986 Jun; 34(6):715-21. PubMed ID: 3531987
[TBL] [Abstract][Full Text] [Related]
13. Mapping the locus for hereditary hemochromatosis: localization between HLA-B and HLA-A.
Edwards CQ; Griffen LM; Dadone MM; Skolnick MH; Kushner JP
Am J Hum Genet; 1986 Jun; 38(6):805-11. PubMed ID: 3460331
[TBL] [Abstract][Full Text] [Related]
14. HLA-A3, B7 linkage disequilibrium in hemochromatotic patients with or without insulin dependent diabetes.
Saddi R; Muller JY; Pouliquen A; Kaplan C; Sylvestre R
Tissue Antigens; 1981 May; 17(5):473-9. PubMed ID: 7336414
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Idiopathic haemochromatosis in the Australian population: HLA linkage and recessivity.
Doran TJ; Bashir HV; Trejaut J; Bassett ML; Halliday JW; Powell LW
Hum Immunol; 1981 May; 2(3):191-200. PubMed ID: 7263316
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. The use of association data to identify family members at high risk for marker-linked diseases.
Conte WJ; Rotter JI
Am J Hum Genet; 1984 Jan; 36(1):152-66. PubMed ID: 6582783
[TBL] [Abstract][Full Text] [Related]
19. Idiopathic hemochromatosis: linkage with HLA.
Lipinski M; Hors J; Saleun JP; Saddi R; Passa P; Lafaurie S; Feingold N; Dausset J
Tissue Antigens; 1978 May; 11(5):471-4. PubMed ID: 694909
[TBL] [Abstract][Full Text] [Related]
20. HLA antigens and haplotypes associated with idiopathic haemochromatosis in Veneto: peculiar association with HLA-A3,B35.
De Menis E; Breda F; Monco A; Foscolo G; Legovini P; Scaldaferri E; Moro L; Conte N
Acta Haematol; 1990; 83(3):113-5. PubMed ID: 2109447
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]