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Results: 5

Authors: Bulman, Dennis E. Murphy, E.Gordon Zubrzycka-Gaarn, Elizabeth E. Worton, Ronald G. Ray, Peter N.
Citation: E. Bulman, Dennis et al., Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophin., American journal of human genetics , 48-I(2), 1991, pp. 295-304

Authors: Grant, Stephen G. Campbell, Christine E. Duff, Catherine Toth, Sandra L. Worton, Ronald G.
Citation: G. Grant, Stephen et al., Gene inactivation as a mechanism for the expression of recessive phenotypes, American journal of human genetics , 45-I(4), 1989, pp. 619-634

Authors: Hu, Xiuyuan Ray, Peter N. Murphy, E. Gordon Thompson, Margaret W. Worton, Ronald G.
Citation: Hu, Xiuyuan et al., Duplicational mutation at the duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotype/genotype correlation, American journal of human genetics , 46-II(4), 1990, pp. 682-695

Authors: Hu, Xiuyuan Burghes, Arthur H. M. Bulman, Dennis E. Ray, Peter N. Worton, Ronald G.
Citation: Hu, Xiuyuan et al., Evidence for mutation by unequal sister chromatid exchange in the duchenne muscular dystrophy gene, American journal of human genetics , 44(6), 1989, pp. 855-863

Authors: MacKenzie, Alex E. Korneluk, Robert G. Zorzato, Francesco Fuji,Junichi Phillips, Michael lles, David Wieringa, Bé Leblond, Suzanne Bailly, Jane Willard, Huntington F. Duff, Catherine Worton, Ronald G. MacLennan, David H.
Citation: E. Mackenzie, Alex et al., The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy, American journal of human genetics , 46-II(6), 1990, pp. 1082-1089
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