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Journal of Medical Genetics|August 1, 1993
A new form of familial ataxia, deafness, and mental retardationW Reardon, J Wilson, N Cavanagh, et al.Journal of Medical Genetics|June 1, 1993
Cerebellar ataxia and ectodermal dysplasia in brothersM Baraitser, W Reardon, A McShane, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
Genetic prediction in Huntington's disease: what are the limitations imposed by pedigree structure?V P Misra, M Baraitser, A E HardingJournal of Medical Genetics|March 1, 1990
A case of atelosteogenesisK Temple, C A Hall, L Chitty, et al.Journal of Medical Genetics|February 1, 1985
Trigonocephaly and the Opitz C syndromeC Sargent, J Burn, M Baraitser, et al.Clinical Dysmorphology|January 1, 1994
Frontofacionasal dysplasia: a new case and review of the phenotypeW Reardon, R M Winter, D Taylor, et al.Clinical Dysmorphology|January 1, 1994
Total situs inversus associated with the oculo-auriculo-vertebral spectrumJ A Maat-Kievit, M Baraitser, R M WinterClinical Dysmorphology|April 1, 1994
Mental retardation, microcephaly and blepharochalasis in brothersW Reardon, R M Winter, J Wilson, et al.American Journal of Medical Genetics|December 11, 1996
Hemihypertrophy, hemimegalencephaly, and polydactylyW Reardon, B Harding, R M Winter, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1981
Biochemical and clinical studies of Friedreich's ataxiaP Purkiss, M Baraitser, O Borud, et al.Pageof 19