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Human Genetics|August 1, 1986
Studies of a DNA marker (G8) genetically linked to Huntington disease in British familiesS Youngman, M Sarfarazi, O W Quarrell, et al.Lancet (London, England)|December 5, 1987
Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophyS M Forrest, T J Smith, G S Cross, et al.Clinical Otolaryngology and Allied Sciences|May 23, 1998
Mucosal melanoma of the head and neckV Nandapalan, N J Roland, T R Helliwell, et al.Journal of Chemical Ecology|December 10, 2013
Toxicity of nitro compounds fromLotus pedunculatus to grass grub (Costelytra zealandica) (Coleoptera: Scarabaeidae)R F Hutchins, O R Sutherland, C Gnanasunderam, et al.The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Mutational analysis in X-linked spondyloepiphyseal dysplasia tardaP T Christie, A Curley, M A Nesbit, et al.Human Antibodies|July 16, 1999
The significance of immune disorder in tropical spastic paraparesisM F Smikle, E N Barton, O C Morgan, et al.Clinical Science (London, England : 1979)|December 1, 1991
Na+/H+ and HCO3-/Cl- exchange in the control of intracellular pH in vivo in the spontaneously hypertensive ratP D Syme, J K Aronson, C H Thompson, et al.Systematic Reviews|September 1, 2016
The range of peripapillary retinal nerve fibre layer and optic disc parameters, in children aged up to but not including 18 years of age who were born prematurely: protocol for a systematic reviewAlexandra L Creavin, Cathy E M Williams, Kate Tilling, et al.Nature Genetics|August 1, 1993
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's diseaseR G Snell, J C MacMillan, J P Cheadle, et al.Genomics|December 1, 1993
Genomic organization and transcriptional units at the myotonic dystrophy locusD J Shaw, M McCurrach, S A Rundle, et al.Pageof 30