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