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Journal Abstract Search

200 related items for PubMed ID: 10431233

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  • 2. 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
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  • 4. A common intron 3 mutation (IVS3 -48c-->g) leads to misdiagnosis of the c.845G-->A (C282Y) HFE gene mutation.
    Beutler E, Gelbart T.
    Blood Cells Mol Dis; 2000 Jun; 26(3):229-33. PubMed ID: 10950943
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  • 9. Uncommon mutations and polymorphisms in the hemochromatosis gene.
    Pointon JJ, Wallace D, Merryweather-Clarke AT, Robson KJ.
    Genet Test; 2000 Jun; 4(2):151-61. PubMed ID: 10953955
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  • 10. Hereditary hemochromatosis in Spain.
    Sánchez M, Bruguera M, Quintero E, Barrio Y, Mazzara R, Rodés J, Oliva R.
    Genet Test; 2000 Jun; 4(2):171-6. PubMed ID: 10953957
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  • 11. Iron beware: a common HFE gene polymorphism may prevent the accurate molecular diagnosis of homozygous hemochromatosis in low-risk, but not high-risk groups.
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    Hepatology; 2000 Feb; 31(2):540-2. PubMed ID: 10655286
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  • 13. Prevalence of the C282Y mutation for haemochromatosis on the Island of Majorca.
    Guix P, Picornell A, Parera M, Tomás C, Muncunill J, Castro JA, Rossell J, Vaquer P, Ramon MM, Obrador A.
    Clin Genet; 2000 Aug; 58(2):123-8. PubMed ID: 11005145
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  • 16. 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
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  • 17. 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
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