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References
Feder, J.N. et al. Nature Genet. 13, 399–408 (1996).
Editorial Nature Genet. 13, 375–376 (1996).
Cox, T. Nature Genet. 13, 386–388 (1996).
Little, P.F.R. Nature 382, 494–495 (1996).
Cartwright, G.E. et al. N. Engl. J. Med. 301, 175–179 (1979).
Simon, M. et al. Gastroenterol. 78, 703–708 (1980).
Powell, L.W. et al. Ann. NY Acad. Sci. 526, 23–33 (1988).
Jazwinska, E.C. et al. Am. J. Hum. Genet. 56, 428–433 (1995).
Gandon, G. et al. Hum. Genet. 97, 103–113 (1996).
Camasohella, C. et al. Hum. Genet. 97, 476–481 (1996).
Worwood, M. et al. Br. J. Haematol. 86, 833–846 (1994).
Seese, N.K. et al. BloodCell. Mol. Dis. 22, 36–46 (1996).
Crawford, D.H.G. et al. Am. J. Hum. Genet. 57, 362–367 (1995).
Burt, J. et al. Genomics 33, 153–158 (1996).
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Jazwinska, E., Cullen, L., Busfield, F. et al. Haemochromatosis and HLA–H. Nat Genet 14, 249–251 (1996). https://doi.org/10.1038/ng1196-249
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DOI: https://doi.org/10.1038/ng1196-249
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