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Scientific Reports|June 24, 2016
Morphology of muscle attachment sites in the modern human hand does not reflect muscle architectureE M Williams-Hatala, K G Hatala, S Hiles, et al.Chest|April 18, 2000
Expiratory airflow patterns in children and adults with cystic fibrosisE M Williams, R G Madgwick, A H Thomson, et al.Developmental Biology|December 16, 1998
The cellular mechanism of epithelial rearrangement during morphogenesis of the Caenorhabditis elegans dorsal hypodermisE M Williams-Masson, P J Heid, C A Lavin, et al.Pharmacology, Biochemistry, and Behavior|December 1, 1996
Prenatal administration of buprenorphine in the rat: effects on the rest-activity cycle at 22 and 30 days of ageD E Hutchings, A S Hamowy, E M Williams, et al.Journal of Medical Genetics|December 1, 1993
Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary choreaJ C MacMillan, P J Morrison, N C Nevin, et al.The British Journal of Ophthalmology|September 1, 1993
Cataract and myotonic dystrophy: the role of molecular diagnosisW Reardon, J C MacMillan, J Myring, et al.The British Journal of Ophthalmology|May 1, 1985
A genetic linkage study of a kindred with X-linked retinitis pigmentosaS S Bhattacharya, J F Clayton, P S Harper, et al.Lancet (London, England)|May 9, 1992
Unstable DNA sequence in myotonic dystrophyH G Harley, S A Rundle, W Reardon, et al.Journal of Medical Genetics|February 1, 1991
Identification of new DNA markers close to the myotonic dystrophy locusJ D Brook, H G Harley, K V Walsh, et al.Human Genetics|May 1, 1993
Charcot-Marie-tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2-->12M Upadhyaya, S H Roberts, J Farnham, et al.Pageof 30