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Human Genetics|January 1, 1990
Genotype-phenotype correlations in XX males and their bearing on current theories of sex determinationM A Ferguson-Smith, A Cooke, N A Affara, et al.Clinical Dysmorphology|January 1, 1993
Severe prenatal infantile cortical hyperostosis (Caffey's disease)P D Turnpenny, R Davidson, E J Stockdale, et al.American Journal of Medical Genetics|May 1, 1987
The Neu-Laxova syndrome in female sibs: clinical and pathological features with prenatal diagnosis in the second sibJ L Tolmie, G Mortimer, D Doyle, et al.Journal of Medical Genetics|October 23, 1998
Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisationS R Ghaffari, E Boyd, J M Connor, et al.Human Genetics|August 1, 1989
Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometryA Cooke, J L Tolmie, J M Colgan, et al.The Journal of Biological Chemistry|December 25, 1982
Resistance to inhibitors of mammalian cell protein synthesis induced by preincubation in hypertonic growth mediumJ R Yates, D L NussCurrent Opinion in Clinical Nutrition and Metabolic Care|September 25, 2001
Proteomics: analytical tools and techniquesM J MacCoss, J R YatesJournal of Medical Genetics|June 3, 1999
Clinical and Molecular genetics of Stickler syndromeM P Snead, J R YatesPageof 56