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Results: 3
A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the hla-a locus and characters required to define a heterozygous population and (2) hypothesis concerning the undelying cause of hemochromatosis-hla association
Authors: Simon, M. Le Mignon, L. Fauchet, R. Yaouanq, J. David, V. Edan, G. Bourel, M.
Citation: M. Simon, et al., A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the hla-a locus and characters required to define a heterozygous population and (2) hypothesis concerning the undelying cause of hemochromatosis-hla association, American journal of human genetics , 41-I(2), 1987, pp. 89-105
Recombinations between IRP and cystic fibrosis
Authors: Farrall, M. Wainwright, B. J. Feldman, G. L. Beaudet, A. Sretenovic, Z. Halley, D. Simon, M. Dickerman, L. Devoto, M. Romeo, G. Kaplan, J.-C. Kitzis, A. Williamson, R.
Citation: M. Farrall, et al., Recombinations between IRP and cystic fibrosis, American journal of human genetics , 43-II(4), 1988, pp. 471-475
Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP
Authors: Simon, M. Phillips, M. Green, H. Stroh, H. Glatt, K. Bruns, G. Latt, S. A.
Citation: M. Simon, et al., Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP, American journal of human genetics , 45-II(6), 1989, pp. 910-916
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