Two Novel Missense Mutations of the HFE Gene (I105T and G93R) and Identification of the S65C Mutation in Alabama Hemochromatosis Probands

By Barton J.C.   Sawada-Hirai R.   Rothenberg B.E.   Acton R.T.  

Blood Cells, Molecules, and Diseases, Vol. 25, Iss. 3, 1999-06 ,pp. : 147-155

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The Hemochromatosis N144H Mutation of SLC11A3 Gene in Patients with Type 2 Diabetes

By Njajou O.T.   Vaessen N.   Oostra B.   Heutink P.   van Duijn C.M.  

Molecular Genetics and Metabolism, Vol. 75, Iss. 3, 2002-03 ,pp. : 290-291

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Commentary: Juvenile Hemochromatosis in a Spanish Family (by Montes-Cano et al.)

By Camaschella C.   Roetto A.   Papanikolaou G.  

Blood Cells, Molecules, and Diseases, Vol. 29, Iss. 1, 2002-01 ,pp. : 83-84

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Genetic and Clinical Description of Hemochromatosis Probands and Heterozygotes: Evidence That Multiple Genes Linked to the Major Histocompatibility Complex Are Responsible for Hemochromatosis

By Barton J.C.   Shih W.W.H.   Sawada-Hirai R.   Acton R.T.   Harmon L.   Rivers C.   Rothenberg B.E.  

Blood Cells, Molecules, and Diseases, Vol. 23, Iss. 1, 1997-04 ,pp. : 135-145

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Significance of Linkage Disequilibrium between Mutation C282Y and a MseI Polymorphism in Population Screening and DNA Diagnosis of Hemochromatosis

By de Villiers J.N.P.   Beutler M.E.J.  

Blood Cells, Molecules, and Diseases, Vol. 25, Iss. 4, 1999-08 ,pp. : 250-252

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