Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy.

Por Bodrug, S E, Holden, J J, Ray, P N, Worton, R G
Publicado em 1991

Cyclin D1 transgene impedes lymphocyte maturation and collaborates in lymphomagenesis with the myc gene.

Por Bodrug, S E, Warner, B J, Bath, M L, Lindeman, G J, Harris, A W, Adams, J M
Publicado em 1994

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

Por Bodrug, S E, Roberson, J R, Weiss, L, Ray, P N, Worton, R G, Van Dyke, D L
Publicado em 1990

Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).

Por Mills, K A, Buetow, K H, Xu, Y, Ritty, T M, Mathews, K D, Bodrug, S E, Wijmenga, C, Balazs, I, Murray, J C
Publicado em 1992

Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter

Por Wijmenga, C., Sandkuijl, L. A., Moerer, P., van der Boorn, N., Bodrug, S. E., Ray, P. N., Brouwer, O. F., Murray, J. C., van Ommen, G. J. B., Padberg, G. W., Frants, R. R.
Publicado em 1992

Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the duchenne muscular dystrophy (DMD) gene

Por Gillard, E. F., Chamberlain, J. S., Murphy, E. G., Duff, C. L., Smith, B., Burghes, A. H. M., Thompson, M. W., Sutherland, J., Oss, I., Bodrug, S. E., Klamut, H. J., Ray, P. N., Worton, R. G.
Publicado em 1989