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.
7. Extreme expansion detection in spinocerebellar ataxia type 2 and type 7. Snow K; Mao R Methods Mol Biol; 2003; 217():41-50. PubMed ID: 12491919 [No Abstract] [Full Text] [Related]
8. Computational prediction of the polyQ and CAG repeat spinocerebellar ataxia network based on sequence identity to untranslated regions. Spence JL; Wallihan S Gene; 2012 Nov; 509(2):273-81. PubMed ID: 22967711 [TBL] [Abstract][Full Text] [Related]
9. Accurate determination of ataxin-2 polyglutamine expansion in patients with intermediate-range repeats. Hussey J; Lockhart PJ; Seltzer W; Wszolek ZK; Payami H; Hanson M; Gwinn-Hardy K; Farrer M Genet Test; 2002; 6(3):217-20. PubMed ID: 12490063 [TBL] [Abstract][Full Text] [Related]
10. Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals. Freund AA; Scola RH; Teive HA; Arndt RC; da Costa-Ribeiro MC; Alle LF; Werneck LC Arq Neuropsiquiatr; 2009 Dec; 67(4):1124-32. PubMed ID: 20069235 [TBL] [Abstract][Full Text] [Related]
11. Caution regarding the interpretation of homoallelism in polyglutamine multiplex assays: a recommendation for confirmatory testing of homozygous alleles. Smith DC; Esterhuizen A; Greenberg J J Mol Diagn; 2013 Sep; 15(5):706-9. PubMed ID: 23871770 [TBL] [Abstract][Full Text] [Related]
13. [Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families]. Song XW; Tang BS; Jiang H; Shen L; Yang Q; Liao SS; Li QH; Liang XC; Tang JG Zhonghua Yi Xue Za Zhi; 2006 Jul; 86(25):1755-8. PubMed ID: 17054842 [TBL] [Abstract][Full Text] [Related]
14. A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array. Holmes SE; Wentzell JS; Seixas AI; Callahan C; Silveira I; Ross CA; Margolis RL Hum Genet; 2006 Sep; 120(2):193-200. PubMed ID: 16783570 [TBL] [Abstract][Full Text] [Related]
15. Large de novo expansion of CAG repeats in patient with sporadic spinocerebellar ataxia type 7. Bauer P; Kraus J; Matoska V; Brouckova M; Zumrova A; Goetz P J Neurol; 2004 Aug; 251(8):1023-4. PubMed ID: 15316811 [No Abstract] [Full Text] [Related]
16. Genotype/phenotype correlation in a SCA1 family: anticipation without CAG expansion. Bauer PO; Matoska V; Zumrova A; Boday A; Doi H; Marikova T; Goetz P J Appl Genet; 2005; 46(3):325-8. PubMed ID: 16110192 [TBL] [Abstract][Full Text] [Related]
17. Late-onset SCA2: 33 CAG repeats are sufficient to cause disease. Matsumura R; Futamura N Neurology; 2001 Aug; 57(3):566. PubMed ID: 11502947 [No Abstract] [Full Text] [Related]
18. Meiotic CAG repeat instability in spinocerebellar ataxia type 6: maternally transmitted elongation in a presumed sporadic case. Lindquist SG; Nørremølle A; Hjermind LE; Hasholt L; Nielsen JE J Neurol Sci; 2006 Feb; 241(1-2):95-8. PubMed ID: 16310805 [TBL] [Abstract][Full Text] [Related]
19. Diagnosis of polyglutamine spinocerebellar ataxias by polymerase chain reaction amplification and Sanger sequencing. Chen C; Fang X; Sun S Mol Med Rep; 2018 Jul; 18(1):1037-1042. PubMed ID: 29845242 [TBL] [Abstract][Full Text] [Related]
20. Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohort. van de Warrenburg BP; Hendriks H; Dürr A; van Zuijlen MC; Stevanin G; Camuzat A; Sinke RJ; Brice A; Kremer BP Ann Neurol; 2005 Apr; 57(4):505-12. PubMed ID: 15747371 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]