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188 related items for PubMed ID: 2317008
21. Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi-point linkage analysis. Kramer PL, Ozelius L, Gusella JF, Fahn S, Kidd KK, Breakefield XO. Genet Epidemiol; 1987; 4(5):377-86. PubMed ID: 3692135 [Abstract] [Full Text] [Related]
22. Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium. Ozelius LJ, Hewett J, Kramer P, Bressman SB, Shalish C, de Leon D, Rutter M, Risch N, Brin MF, Markova ED, Limborska SA, Ivanova-Smolenskaya IA, McCormick MK, Fahn S, Buckler AJ, Gusella JF, Breakefield XO. Genome Res; 1997 May; 7(5):483-94. PubMed ID: 9149944 [Abstract] [Full Text] [Related]
24. Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South Tyrol. Klein C, Pramstaller PP, Castellan CC, Breakefield XO, Kramer PL, Ozelius LJ. Ann Neurol; 1998 Sep; 44(3):394-8. PubMed ID: 9749609 [Abstract] [Full Text] [Related]