These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
167 related articles for article (PubMed ID: 3477955)
1. Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6. Rich SS; Wilkie P; Schut L; Vance G; Orr HT Am J Hum Genet; 1987 Oct; 41(4):524-31. PubMed ID: 3477955 [TBL] [Abstract][Full Text] [Related]
2. Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6. Haines JL; Trofatter JA Genet Epidemiol; 1986; 3(6):399-405. PubMed ID: 3468044 [TBL] [Abstract][Full Text] [Related]
3. Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis. Zoghbi HY; Sandkuyl LA; Ott J; Daiger SP; Pollack M; O'Brien WE; Beaudet AL Am J Hum Genet; 1989 Feb; 44(2):255-63. PubMed ID: 2563195 [TBL] [Abstract][Full Text] [Related]
4. Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locus. Twells R; Yenchitsomanus PT; Sirinavin C; Allotey R; Poungvarin N; Viriyavejakul A; Cemal C; Weber J; Farrall M; Rodprasert P Hum Mol Genet; 1994 Jan; 3(1):177-80. PubMed ID: 8162021 [TBL] [Abstract][Full Text] [Related]
5. Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindred. Ranum LP; Rich SS; Nance MA; Duvick LA; Aita JF; Orr HT; Anton-Johnson S; Schut LJ Neurology; 1992 Feb; 42(2):344-7. PubMed ID: 1736163 [TBL] [Abstract][Full Text] [Related]
6. Adult onset spinocerebellar ataxia linked to HLA in a South African kindred of mixed ancestry. Bryer A; Martell RW; du Toit ED; Beighton P Tissue Antigens; 1992 Sep; 40(3):111-5. PubMed ID: 1440565 [TBL] [Abstract][Full Text] [Related]
7. Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p. Ranum LP; Duvick LA; Rich SS; Schut LJ; Litt M; Orr HT Am J Hum Genet; 1991 Jul; 49(1):31-41. PubMed ID: 1676561 [TBL] [Abstract][Full Text] [Related]
8. Spinocerebellar ataxia: multipoint linkage analysis of genes associated with the disease locus. Wilkie PJ; Schut LJ; Rich SS Hum Genet; 1991 Aug; 87(4):405-8. PubMed ID: 1879827 [TBL] [Abstract][Full Text] [Related]
9. The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds. Zoghbi HY; Jodice C; Sandkuijl LA; Kwiatkowski TJ; McCall AE; Huntoon SA; Lulli P; Spadaro M; Litt M; Cann HM Am J Hum Genet; 1991 Jul; 49(1):23-30. PubMed ID: 2063871 [TBL] [Abstract][Full Text] [Related]
10. Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region. Lopes-Cendes I; Andermann E; Attig E; Cendes F; Bosch S; Wagner M; Gerstenbrand F; Andermann F; Rouleau GA Am J Hum Genet; 1994 May; 54(5):774-81. PubMed ID: 8178818 [TBL] [Abstract][Full Text] [Related]
11. Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population. Auburger G; Diaz GO; Capote RF; Sanchez SG; Perez MP; del Cueto ME; Meneses MG; Farrall M; Williamson R; Chamberlain S Am J Hum Genet; 1990 Jun; 46(6):1163-77. PubMed ID: 1971152 [TBL] [Abstract][Full Text] [Related]
12. HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds. Spadaro M; Giunti P; Lulli P; Frontali M; Jodice C; Cappellacci S; Morellini M; Persichetti F; Trabace S; Anastasi R Acta Neurol Scand; 1992 Apr; 85(4):257-65. PubMed ID: 1585797 [TBL] [Abstract][Full Text] [Related]
13. Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded. Keats BJ; Pollack MS; McCall A; Wilensky MA; Ward LJ; Lu M; Zoghbi HY Am J Hum Genet; 1991 Nov; 49(5):972-7. PubMed ID: 1928103 [TBL] [Abstract][Full Text] [Related]
14. Regional mapping of the gene for autosomal dominant spinocerebellar ataxia (SCA1) by localizing the closely linked D6S89 locus to 6p24.2----p23.05. Volz A; Fonatsch C; Ziegler A Cytogenet Cell Genet; 1992; 60(1):37-9. PubMed ID: 1582256 [TBL] [Abstract][Full Text] [Related]
15. Autosomal dominant spinocerebellar ataxia (SCA) in a Siberian founder population: assignment to the SCA1 locus. Lunkes A; Goldfarb LG; Platonov FA; Alexeev VP; Duenas-Barajas E; Gajdusek DC; Auburger G Exp Neurol; 1994 Apr; 126(2):310-2. PubMed ID: 7925830 [TBL] [Abstract][Full Text] [Related]
16. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1. Gispert S; Twells R; Orozco G; Brice A; Weber J; Heredero L; Scheufler K; Riley B; Allotey R; Nothers C Nat Genet; 1993 Jul; 4(3):295-9. PubMed ID: 8358438 [TBL] [Abstract][Full Text] [Related]
17. Machado Joseph disease is not an allele of the spinocerebellar ataxia 2 locus. Twist EC; Farrer LA; Macleod PM; Radvany J; Chamberlain S; Rosenberg RN; Rouleau GA Hum Genet; 1994 Mar; 93(3):335-8. PubMed ID: 8125487 [TBL] [Abstract][Full Text] [Related]
18. The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1). Carson WJ; Radvany J; Farrer LA; Vincent D; Rosenberg RN; MacLeod PM; Rouleau GA Genomics; 1992 Jul; 13(3):852-5. PubMed ID: 1639414 [TBL] [Abstract][Full Text] [Related]
19. Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy. Matsuura T; Achari M; Khajavi M; Bachinski LL; Zoghbi HY; Ashizawa T Ann Neurol; 1999 Mar; 45(3):407-11. PubMed ID: 10072060 [TBL] [Abstract][Full Text] [Related]
20. Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindred. Zoghbi HY; Pollack MS; Lyons LA; Ferrell RE; Daiger SP; Beaudet AL Ann Neurol; 1988 Jun; 23(6):580-4. PubMed ID: 3165612 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]