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Results: 1-3 |
Results: 3
Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B
Authors: Ludwig, M. Schwaab, R. Eigel, A. Horst, J. Egli, H. Brackman, H.-H. Olek, K.
Citation: M. Ludwig, et al., Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B, American journal of human genetics , 45-I(1), 1989, pp. 115-122
Parental origin of factor IX gene mutations, and their distribution in the gene.
Authors: Ludwig, M. Grimm, T. Brackmann, H. H. Olek, K.
Citation: M. Ludwig, et al., Parental origin of factor IX gene mutations, and their distribution in the gene., American journal of human genetics , 50-I(1), 1992, pp. 164-173
Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome
Authors: Zengerling, S. Tsui, L.C. Grzeschik, K. Olek, K. Riordan, J.R.
Citation: S. Zengerling, et al., Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome, American journal of human genetics , 40(3), 1987, pp. 228-236
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