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Brain Pathology (Zurich, Switzerland)|July 1, 1997
Toward understanding the molecular pathology of Huntington's diseaseC L Wellington, R R Brinkman, J R O'Kusky, et al.Clinical Genetics|July 22, 2014
Use of genetic technologies to compare medicinesS E Kolitz, F Towfic, I Grossman, et al.American Journal of Human Genetics|April 17, 1999
A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington diseaseE W Almqvist, M Bloch, R Brinkman, et al.American Journal of Human Genetics|October 1, 1992
The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosaO Riess, A Noerremoelle, B Weber, et al.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 6, 1987
Molecular genetics and Huntington's disease. The South African situationM R Hayden, J Goldblatt, G Wallis, et al.Clinical Genetics|October 12, 2001
High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British ColumbiaE W Almqvist, D S Elterman, P M MacLeod, et al.American Journal of Medical Genetics|July 1, 1989
Epiphyseal dysplasia, microcephaly, nystagmus, and retinitis pigmentosaR B Lowry, B J Wood, T A Cox, et al.Clinical Genetics|October 9, 2012
Providing predictive testing for Huntington disease via telehealth: results of a pilot study in British Columbia, CanadaA K Hawkins, S Creighton, A Ho, et al.Clinical Biochemistry|April 1, 1985
Urinary proteins in a patient with Tangier diseaseP H Pritchard, M Bergseth, R McLeod, et al.Brain Research|March 20, 1999
Neuronal degeneration in the basal ganglia and loss of pallido-subthalamic synapses in mice with targeted disruption of the Huntington's disease geneJ R O'Kusky, J Nasir, F Cicchetti, et al.Pageof 34