Incidence of salt-losing form of congenital virilizing adrenal hyperplasia.

Por Qazi, Q H, Thompson, M W
Publicado em 1972

Carrier detection and genetic counselling in Duchenne muscular dystrophy: a follow-up study.

Por Hutton, E. M., Thompson, M. W.
Publicado em 1976

Intelligence and the gene for Duchenne muscular dystrophy.

Por Prosser, E. J., Murphy, E. G., Thompson, M. W.
Publicado em 1969

ATOMIC COLLISION PHENOMENA IN SOLIDS.

Por THOMPSON M W., PALMER D W., TOWNSEND P D.
Publicado em S1970

Genetics of childhood spinal muscular atrophy.

Por Winsor, E J, Murphy, E G, Thompson, M W, Reed, T E
Publicado em 1971

Moderate- and high-intensity exhaustive exercise in the heat induce a similar increase in monocyte Hsp72

Por Périard, J. D., Ruell, P. A., Thompson, M. W., Caillaud, C.
Publicado no Cell Stress Chaperones (2015)

Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlation.

Por Hu, X Y, Ray, P N, Murphy, E G, Thompson, M W, Worton, R G
Publicado em 1990

Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.

Por Thompson, M W, Ray, P N, Belfall, B, Duff, C, Logan, C, Oss, I, Worton, R G
Publicado em 1986

Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy.

Por Kean, V M, Macleod, H L, Thompson, M W, Ray, P N, Verellen-Dumoulin, C, Worton, R G
Publicado em 1986

Partial gene duplication in Duchenne and Becker muscular dystrophies.

Por Hu, X Y, Burghes, A H, Ray, P N, Thompson, M W, Murphy, E G, Worton, R G
Publicado em 1988

The influence of menstrual cycle phase on skeletal muscle contractile characteristics in humans

Por de Jonge, X A K Janse, Boot, C R L, Thom, J M, Ruell, P A, Thompson, M W
Publicado em 2001

Chronic hypertension and altered baroreflex responses in transgenic mice containing the human renin and human angiotensinogen genes.

Por Merrill, D C, Thompson, M W, Carney, C L, Granwehr, B P, Schlager, G, Robillard, J E, Sigmund, C D
Publicado em 1996

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