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Journal Abstract Search

99 related items for PubMed ID: 12651261

  • 81. 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
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  • 84. Inherited iron overload disorders.
    Piperno A, Pelucchi S, Mariani R.
    Transl Gastroenterol Hepatol; 2020 Apr; 5():25. PubMed ID: 32258529
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  • 87. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
    Cukjati M, Vaupotic T, Rupreht R, Curin-Serbec V.
    BMC Med Genet; 2007 Nov 23; 8():69. PubMed ID: 18036208
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  • 93. Prevalence of C282Y and E168X HFE mutations in an Italian population of Northern European ancestry.
    Salvioni A, Mariani R, Oberkanins C, Moritz A, Mauri V, Pelucchi S, Riva A, Arosio C, Cerutti P, Piperno A.
    Haematologica; 2003 Mar 23; 88(3):250-5. PubMed ID: 12651261
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  • 97. Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain.
    Altes A, Ruiz A, Barceló MJ, Remacha AF, Puig T, Maya AJ, Castell C, Amate JM, Saz Z, Baiget M.
    Genet Test; 2004 Mar 23; 8(4):407-10. PubMed ID: 15684872
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