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Journal of Inherited Metabolic Disease|January 1, 1981
Studies on human phenylalanine Mono-oxygenase. I. Restricted expressionM D Crawfurd, D A Gibbs, D M SheppardJournal of Medical Genetics|October 1, 1979
Brachydactyly and polydactyly with dermal ridge dissociation and ridge hypoplasiaM D Crawfurd, P Saldaña-GarciaLancet (London, England)|November 24, 1984
First-trimester diagnosis of Lesch-Nyhan syndromeD A Gibbs, I R McFadyen, M D Crawfurd, et al.Annals of Allergy|May 1, 1976
Inhibition of gill cilial activity and of Proteus vulgaris motility as tests for aspirin idiosyncrasyJ C Delaney, M D Crawfurd, C RobertsJournal of Medical Genetics|October 1, 1979
Non-progressive cerebellar ataxia, aplasia of pupillary zone of iris, and mental subnormality (Gillespie's syndrome) affecting 3 members of a non-consanguineous family in 2 generationsM D Crawfurd, R B Harcourt, P A ShawPrenatal Diagnosis|June 1, 1991
Interstitial deletions without phenotypic effect: prenatal diagnosis of a new family and brief reviewJ C Barber, H Mahl, J Portch, et al.Journal of Medical Genetics|June 1, 1990
A further family with congenital renal proximal tubular dysgenesisP MacMahon, R A Blackie, M J House, et al.Brain and Language|June 17, 2000
The neurodevelopmental frontostriatal disorders: evolutionary adaptiveness and anomalous lateralizationJ L Bradshaw, D M SheppardPageof 5