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24. A multistep mutation mechanism drives the evolution of the CAG repeat at MJD/SCA3 locus. Martins S; Calafell F; Wong VC; Sequeiros J; Amorim A Eur J Hum Genet; 2006 Aug; 14(8):932-40. PubMed ID: 16724006 [TBL] [Abstract][Full Text] [Related]
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26. Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) families. Iughetti P; Otto PA; Zatz M; Passos Bueno MR; Marie SK Am J Med Genet; 1998 May; 77(3):246-8. PubMed ID: 9605593 [No Abstract] [Full Text] [Related]
27. Machado-Joseph disease and other rare spinocerebellar ataxias. Matilla-Dueñas A Adv Exp Med Biol; 2012; 724():172-88. PubMed ID: 22411243 [TBL] [Abstract][Full Text] [Related]
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32. [Detection of the CAG trinucleotide repeats of MJD1 gene by recombinant DNA technology]. Zhang S; Wang JL; Xu Q; Li XH; Lei LF; Jiang H; Shen L; Yan XX; Pan Q; Xia K; Tang BS Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):406-9. PubMed ID: 20017304 [TBL] [Abstract][Full Text] [Related]
33. Prenatal diagnosis of Machado-Joseph disease/Spinocerebellar Ataxia Type 3 in Taiwan: early detection of expanded ataxin-3. Tsai HF; Liu CS; Chen GD; Lin ML; Li C; Chen YY; Wang BT; Hsieh M J Clin Lab Anal; 2003; 17(5):195-200. PubMed ID: 12938149 [TBL] [Abstract][Full Text] [Related]
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35. 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]
36. Mosaicism of the CAG repeat in CNS tissue in relation to age at death in spinocerebellar ataxia type 1 and Machado-Joseph disease patients. Maciel P; Lopes-Cendes I; Kish S; Sequeiros J; Rouleau GA Am J Hum Genet; 1997 Apr; 60(4):993-6. PubMed ID: 9106546 [No Abstract] [Full Text] [Related]
37. An improved polymerase chain reaction method for genetic testing of spinocerebellar ataxia type 3. Sun WP; He XH; Yu LQ; Wang DP; Qin ZhH; Fang Q; Wang J Genetika; 2011 Oct; 47(10):1416-9. PubMed ID: 22232931 [TBL] [Abstract][Full Text] [Related]
38. Mendelian segregation of normal CAG trinucleotide repeat alleles at three autosomal loci. MacMillan JC; Voisey J; Healey SC; Martin NG J Med Genet; 1999 Mar; 36(3):258-9. PubMed ID: 10204858 [TBL] [Abstract][Full Text] [Related]
39. Improvement in the molecular diagnosis of Machado-Joseph disease. Maciel P; Costa MC; Ferro A; Rousseau M; Santos CS; Gaspar C; Barros J; Rouleau GA; Coutinho P; Sequeiros J Arch Neurol; 2001 Nov; 58(11):1821-7. PubMed ID: 11708990 [TBL] [Abstract][Full Text] [Related]
40. The repeat expansion detection method in the analysis of diseases with CAG/CTG repeat expansion: usefulness and limitations. Martorell L; Pujana MA; Volpini V; Sanchez A; Joven J; Vilella E; Estivill X Hum Mutat; 1997; 10(6):486-8. PubMed ID: 9401013 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]