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Restorative Neurology and Neuroscience|July 24, 2004
Connection between p53 gene Bam HI RFLP polymorphism with the volume of brain infarction in patients with carotid atherothrombotic ischemic strokeV I Skvortsova, P A Slominsky, L V Gubskii, et al.
European Journal of Neurology|March 29, 2007
A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in RussiaS N Illarioshkin, M I Shadrina, P A Slominsky, et al.
Cerebellum & Ataxias|January 16, 2016
ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxiaM I Shadrina, M V Shulskaya, S A Klyushnikov, et al.
Gene|April 27, 1999
Fine mapping of a polymorphic CA repeat marker on human chromosome 19 and its use in population studiesO V Belyaeva, O P Balanovsky, L K Ashworth, et al.
Human Molecular Genetics|June 9, 1998
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystoniaC Klein, M F Brin, D de Leon, et al.
Annals of Human Biology|March 27, 2007
Polymorphisms at locus D1S80 and other hypervariable regions in the analysis of Eastern European ethnic group relationshipsD A Verbenko, P A Slominsky, V A Spitsyn, et al.
Brain : a Journal of Neurology|December 1, 1996
Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophyS N Illarioshkin, I A Ivanova-Smolenskaya, H Tanaka, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
Polymorphism of trinucleotide repeats in loci DM, DRPLA and SCA1 in East European populationsS N Popova, P A Slominsky, E A Pocheshnova, et al.
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