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Clinical Dysmorphology|April 1, 1997
A syndrome of brachyphalangy, polydactyly and absent tibiaeM Baraitser, F Stewart, R M Winter, et al.
Journal of Medical Genetics|March 1, 1989
Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studiesM A Patton, F Giannelli, A J Francis, et al.
Journal of Medical Genetics|September 1, 1989
Moebius' syndrome with unilateral cerebellar hypoplasiaM G Harbord, J P Finn, M A Hall-Craggs, et al.
Neuropediatrics|August 1, 1989
Early onset leukodystrophy with distinct facial features in 2 siblingsM G Harbord, J P Finn, M A Hall-Craggs, et al.
Journal of Child Neurology|April 1, 1993
Alexander's disease: clues to diagnosisC L Pridmore, M Baraitser, B Harding, et al.
Journal of Medical Genetics|September 1, 1991
A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndromeM Ireland, C English, I Cross, et al.
Neuroscience Letters|March 31, 2015
Variation in complement protein C1q is not a major contributor to cognitive impairment in Parkinson's diseaseSophia Carbutt, Jennifer Duff, Alison Yarnall, et al.
Journal of Parkinson'S Disease|August 14, 2013
Guided self-help for the management of worry in Parkinson's disease: a pilot studyRachael A Lawson, David Millar, Richard G Brown, et al.
Clinical Rehabilitation|December 20, 2007
How do I sound to me? Perceived changes in communication in Parkinson's diseaseNick Miller, Emma Noble, Diana Jones, et al.
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