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European Journal of Human Genetics : EJHG|January 1, 1993
A five-year prospective study of the health of children in different ethnic groups, with particular reference to the effect of inbreedingS Bundey, H AlamBrain : a Journal of Neurology|September 1, 1975
A clinical and genetic study of chronic proximal spinal muscular atrophyS Bundey, R E LovelaceAmerican Journal of Human Genetics|January 1, 1983
Spontaneous expression of the chromosome fragile site fra(10)(q25)A M Taylor, S BundeyJournal of Medical Genetics|December 1, 1984
A study of retinitis pigmentosa in the City of Birmingham. I PrevalenceS Bundey, S J CrewsJournal of Medical Genetics|December 1, 1984
A study of retinitis pigmentosa in the City of Birmingham. II Clinical and genetic heterogeneityS Bundey, S J CrewsJournal of the Royal Society of Medicine|July 1, 1989
Ten years experience of a genetic eye clinic: 1978-1987S Bundey, S J CrewsClinical Genetics|September 1, 1990
Very early onset Huntington's disease: genetic mechanism and risk to siblingsD J Clarke, S BundeyDevelopmental Medicine and Child Neurology|April 1, 1977
Recurrence risks in families of children with symmetrical spasticityS Bundey, M I GriffithsJournal of Mental Deficiency Research|February 1, 1991
A family with three sisters with the 4p- syndrome, originally reported as suffering from the Smith-Lemli-Opitz syndromeS Hill, M Creasy, S BundeyJournal of Mental Deficiency Research|February 1, 1990
Folate treatment of a boy with fragile-X syndromeT Webb, P Crawley, S BundeyPageof 8