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Molecular Carcinogenesis|June 1, 1997
A deletion polymorphism due to Alu-Alu recombination in intron 2 of the retinoblastoma gene: association with human gliomasP G Rothberg, S Ponnuru, D Baker, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|April 25, 2001
Autosomal dominant Stargardt-like macular dystrophy: founder effect and reassessment of genetic heterogeneityL A Donoso, A T Frost, E M Stone, et al.Human Genetics|September 10, 1999
Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutationsD A Pillers, K M Fitzgerald, N M Duncan, et al.Pageof 6