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7. Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy. Belsham DD; Yee WC; Greenberg CR; Wrogemann K J Neurol Sci; 1992 Oct; 112(1-2):133-8. PubMed ID: 1469423 [TBL] [Abstract][Full Text] [Related]
8. Somatic stability of the expanded CAG trinucleotide repeat in X-linked spinal and bulbar muscular atrophy. Spiegel R; La Spada AR; Kress W; Fischbeck KH; Schmid W Hum Mutat; 1996; 8(1):32-7. PubMed ID: 8807333 [TBL] [Abstract][Full Text] [Related]
10. Polymorphic CAG repeat length in the androgen receptor gene and association with neurodegeneration in a heterozygous female carrier of Kennedy's disease. Greenland KJ; Beilin J; Castro J; Varghese PN; Zajac JD J Neurol; 2004 Jan; 251(1):35-41. PubMed ID: 14999487 [TBL] [Abstract][Full Text] [Related]
11. Preimplantation Genetic Testing for Monogenic Disease of Spinal Muscular Atrophy by Multiple Displacement Amplification: 11 unaffected livebirths. Fu Y; Shen X; Wu H; Chen D; Zhou C Int J Med Sci; 2019; 16(9):1313-1319. PubMed ID: 31588198 [No Abstract] [Full Text] [Related]
12. [Somatic mosaicism of expanded CAG trinucleotide repeat in spinal and bulbar muscular atrophy (SBMA)]. Tanaka F; Ito Y; Sobue G Nihon Rinsho; 1999 Apr; 57(4):862-8. PubMed ID: 10222780 [TBL] [Abstract][Full Text] [Related]
13. Pathogenesis and therapy of spinal and bulbar muscular atrophy (SBMA). Katsuno M; Tanaka F; Adachi H; Banno H; Suzuki K; Watanabe H; Sobue G Prog Neurobiol; 2012 Dec; 99(3):246-56. PubMed ID: 22609045 [TBL] [Abstract][Full Text] [Related]
14. CAG repeat length variation in sperm from a patient with Kennedy's disease. Zhang L; Fischbeck KH; Arnheim N Hum Mol Genet; 1995 Feb; 4(2):303-5. PubMed ID: 7757084 [TBL] [Abstract][Full Text] [Related]
15. Clinical applications of MARSALA for preimplantation genetic diagnosis of spinal muscular atrophy. Ren Y; Zhi X; Zhu X; Huang J; Lian Y; Li R; Jin H; Zhang Y; Zhang W; Nie Y; Wei Y; Liu Z; Song D; Liu P; Qiao J; Yan L J Genet Genomics; 2016 Sep; 43(9):541-547. PubMed ID: 27599922 [TBL] [Abstract][Full Text] [Related]
16. Case report: birth after preimplantation genetic diagnosis of a subtle mutation in SMN1 gene. Moutou C; Machev N; Gardes N; Viville S Prenat Diagn; 2006 Nov; 26(11):1037-41. PubMed ID: 16941715 [TBL] [Abstract][Full Text] [Related]
17. [Clinical manifestations and molecular genetics of spinal bulbar muscular atrophy: report of 5 cases]. Li XH; Zhuang JJ; Xie QY; Li AP; Liang XL; Feng YQ; Fang YY; Li JR; Liang YX Zhonghua Yi Xue Za Zhi; 2007 Jun; 87(23):1611-5. PubMed ID: 17803850 [TBL] [Abstract][Full Text] [Related]
18. Mitotic and meiotic stability of the CAG repeat in the X-linked spinal and bulbar muscular atrophy gene. Watanabe M; Abe K; Aoki M; Yasuo K; Itoyama Y; Shoji M; Ikeda Y; Iizuka T; Ikeda M; Shizuka M; Mizushima K; Hirai S Clin Genet; 1996 Sep; 50(3):133-7. PubMed ID: 8946111 [TBL] [Abstract][Full Text] [Related]
19. Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy. Igarashi S; Tanno Y; Onodera O; Yamazaki M; Sato S; Ishikawa A; Miyatani N; Nagashima M; Ishikawa Y; Sahashi K Neurology; 1992 Dec; 42(12):2300-2. PubMed ID: 1461383 [TBL] [Abstract][Full Text] [Related]
20. [A novel primer extension method to detect the number of CAG repeats in the androgen receptor gene in families with X-linked spinal and bulbar muscular atrophy]. Sakoda S; Yamamoto Y Nihon Rinsho; 1993 Sep; 51(9):2414-9. PubMed ID: 8411722 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]