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Human Genetics|December 24, 1997
Inv(10)(p11.2q21.2), a variant chromosomeM N Collinson, A M Fisher, J Walker, et al.Genetical Research|October 1, 1990
The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysisD O Robinson, Y Boyd, D Cockburn, et al.American Journal of Medical Genetics|March 1, 1996
Unbalanced translocation in a mother and her son in one of two 5;10 translocation familiesJ C Barber, I K Temple, P L Campbell, et al.Journal of Medical Genetics|June 27, 1998
Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significanceJ C Barber, C A Joyce, M N Collinson, et al.Pageof 1