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Journal of Medical Genetics|April 1, 1989
The recurrence risks for mild idiopathic mental retardationS Bundey, A Thake, J ToddJournal of Medical Genetics|August 1, 1993
Is skewed X inactivation responsible for symptoms in female carriers for adrenoleucodystrophy?E Watkiss, T Webb, S BundeyThe Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1974
Large electroencephalographic responses and their relationship to cleido-cranial dysplasiaA Upton, S Bundey, S SandersJournal of Medical Genetics|April 1, 1982
Family studies on the chromosomal location of the retinoblastoma gene (Rb-1)J Morten, D G Harnden, S BundeyPrenatal Diagnosis|November 1, 1989
Missed prenatal diagnosis of fragile-X syndromeT P Webb, S Bundey, M McKinleyArchives of Disease in Childhood|November 1, 1985
Is it possible to make a clinical diagnosis of the fragile X syndrome in a boy?A Thake, J Todd, S Bundey, et al.Journal of Medical Genetics|February 1, 1992
Multiple mutation in an extended Duchenne muscular dystrophy familyA Miciak, A Keen, D Jadayel, et al.Journal of Medical Genetics|March 1, 1975
A genetic study of torsion dystoniaS Bundey, M J Harrison, C D MarsdenJournal of Neurology, Neurosurgery, and Psychiatry|June 1, 1970
Early recognition of heterozygotes for the gene for dystrophia myotonicaS Bundey, C O Carter, J F SoothillDevelopmental Medicine and Child Neurology|December 1, 1987
Children with the fragile X chromosome at schools for the mildly mentally retardedA Thake, J Todd, T Webb, et al.Pageof 84