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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.
Prenatal Diagnosis|February 1, 1987
Prenatal diagnosis of alpha-1-antitrypsin deficiency by fetal blood samplingG Corney, D B Whitehouse, D A Hopkinson, et al.
American Journal of Medical Genetics|September 1, 1990
Midline facial defects with ocular colobomataI K Temple, H Brunner, B Jones, 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.
Molecular and Cellular Probes|October 1, 1996
Mutation detection in exons 1-14 of the adenomatous polyposis coli gene: identification of an alternatively spliced transcriptT Hamzehloei, S P West, P Chapman, et al.
Headache|March 1, 1993
An association between migrainous aura and hereditary haemorrhagic telangiectasiaJ G Steele, P U Nath, J Burn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2004
Frequency of orthostatic hypotension in a community based cohort of patients with Parkinson's diseaseL M Allcock, K Ullyart, R A Kenny, et al.
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