Hereditary Hemochromatosis - Life Sciences bibliographies - in Harvard style

In-text: (Adams and Barton, 2007)

Your Bibliography: Adams, P. and Barton, J., 2007. Hemochromatosis. The Lancet, 370(9602), pp.1855-1860.

In-text: (Barton and Bertoli, 1996)

Your Bibliography: Barton, J. and Bertoli, L., 1996. Hemochromatosis: The genetic disorder of the twenty–first century. Nat Med, 2(4), pp.394-395.

In-text: (Barton, Sawada-Hirai, Rothenberg and Acton, 1999)

Your Bibliography: Barton, J., Sawada-Hirai, R., Rothenberg, B. and Acton, R., 1999. Two Novel Missense Mutations of the HFE Gene (I105T and G93R) and Identification of the S65C Mutation in Alabama Hemochromatosis Probands. Blood Cells, Molecules, and Diseases, 25(3), pp.147-155.

In-text: (Beutler et al., 1996)

Your Bibliography: Beutler, E., Gelbart, T., West, C., Lee, P., Adams, M., Blackstone, R., Pockros, P., Kosty, M., Venditti, C., Phatak, P., Seese, N., Chorney, K., Ten Elshof, A., Gerhard, G. and Chorney, M., 1996. Mutation Analysis in Hereditary Hemochromatosis. Blood Cells, Molecules, and Diseases, 22(2), pp.187-194.

In-text: (Borecki et al., 1990)

Your Bibliography: Borecki, I., Lathrop, G., Bonney, G., Yaouanq, J. and Rao, D., 1990. Combined Segregation and Linkage Analysis of Genetic Hemochromatosis Using Affection Status, Serum Iron, and HLA. American Journal of Human Genetics, 47(3), pp.542-550.

In-text: (Desforges, Edwards and Kushner, 1993)

Your Bibliography: Desforges, J., Edwards, C. and Kushner, J., 1993. Screening for Hemochromatosis. New England Journal of Medicine, 328(22), pp.1616-1620.

In-text: (Feder et al., 1996)

Your Bibliography: Feder, J., Gnirke, A., Thomas, W., Tsuchihashi, Z., Ruddy, D., Basava, A., Dormishian, F., Domingo, R., Ellis, M., Fullan, A., Hinton, L., Jones, N., Kimmel, B., Kronmal, G., Lauer, P., Lee, V., Loeb, D., Mapa, F., McClelland, E., Meyer, N., Mintier, G., Moeller, N., Moore, T., Morikang, E., Prass, C., Quintana, L., Starnes, S., Schatzman, R., Brunke, K., Drayna, D., Risch, N., Bacon, B. and Wolff, R., 1996. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis. Nat Genet, 13(4), pp.399-408.

In-text: (Feder et al., 1997)

Your Bibliography: Feder, J., Tsuchihashi, Z., Irrinki, A., Lee, V., Mapa, F., Morikang, E., Prass, C., Starnes, S., Wolff, R., Parkkila, S., Sly, W. and Schatzman, R., 1997. The Hemochromatosis Founder Mutation in HLA-H Disrupts  2-Microglobulin Interaction and Cell Surface Expression. Journal of Biological Chemistry, 272(22), pp.14025-14028.

In-text: (Welcome, 2015)

Your Bibliography: Hemochromatosis.org - An Education Website for Hemochromatosis and Too Much Iron. 2015. Welcome. [online] Available at: <http://www.hemochromatosis.org/#diagnosis> [Accessed 15 March 2015].

In-text: (Hussain et al., 2000)

Your Bibliography: Hussain, S., Raja, K., Amstad, P., Sawyer, M., Trudel, L., Wogan, G., Hofseth, L., Shields, P., Billiar, T., Trautwein, C., Hohler, T., Galle, P., Phillips, D., Markin, R., Marrogi, A. and Harris, C., 2000. Increased p53 mutation load in nontumorous human liver of Wilson disease and hemochromatosis: Oxyradical overload diseases. Proceedings of the National Academy of Sciences, 97(23), pp.12770-12775.

In-text: (Jazwinska, 1997)

Your Bibliography: Jazwinska, E., 1997. Hemochromatosis and "HLA-H": Definite!. Hepatology, 25(2), pp.495-496.

In-text: (Lebrón et al., 1998)

Your Bibliography: Lebrón, J., Bennett, M., Vaughn, D., Chirino, A., Snow, P., Mintier, G., Feder, J. and Bjorkman, P., 1998. Crystal Structure of the Hemochromatosis Protein HFE and Characterization of Its Interaction with Transferrin Receptor. Cell, 93(1), pp.111-123.

In-text: (Merryweather-Clarke, Pointon, Shearman and Robson, 1997)

Your Bibliography: Merryweather-Clarke, A., Pointon, J., Shearman, J. and Robson, K., 1997. Global prevalence of putative haemochromatosis mutations. Journal of Medical Genetics, 34(4), pp.275-278.

In-text: (Parkkila et al., 1997)

Your Bibliography: Parkkila, S., Waheed, A., Britton, R., Feder, J., Tsuchihashi, Z., Schatzman, R., Bacon, B. and Sly, W., 1997. Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract. Proceedings of the National Academy of Sciences, 94(6), pp.2534-2539.

In-text: (Pietrangelo, 2006)

Your Bibliography: Pietrangelo, A., 2006. Hereditary hemochromatosis. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1763(7), pp.700-710.

In-text: (Santos, 1997)

Your Bibliography: Santos, M., 1997. Defective iron homeostasis in β-microglobulin knockout mice recapitulates hereditary hemochromatosis in man. Immunology Letters, 56(1-3), p.239.

In-text: (Stevens, Walters, Watt and McCarthy, 1977)

Your Bibliography: Stevens, F., Walters, J., Watt, D. and McCarthy, C., 1977. Inheritance of idiopathic haemochromatosis. Lancet, 309, pp.1106-1107.

In-text: (Valberg and Ghent, 1985)

Your Bibliography: Valberg, L. and Ghent, C., 1985. Diagnosis and Management of Hereditary Hemochromatosis. Annu. Rev. Med., 36(1), pp.27-37.

In-text: (Waheed et al., 1997)

Your Bibliography: Waheed, A., Parkkila, S., Zhou, X., Tomatsu, S., Tsuchihashi, Z., Feder, J., Schatzman, R., Britton, R., Bacon, B. and Sly, W., 1997. Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with  2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells. Proceedings of the National Academy of Sciences, 94(23), pp.12384-12389.

In-text: (Willis, 2000)

Your Bibliography: Willis, G., 2000. Incidence of liver disease in people with HFE mutations. Gut, 46(3), pp.401-404.