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7. 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]
8. [DNA diagnosis of X-linked recessive bulbospinal muscular atrophy by androgen receptor gene mutations]. Doyu M; Sobue G; Mukai E; Takahashi A; Mitsuma T Rinsho Shinkeigaku; 1992 Mar; 32(3):336-9. PubMed ID: 1628462 [TBL] [Abstract][Full Text] [Related]
9. Molecular analysis of the androgen receptor gene in Kennedy's disease. Report of two families and review of the literature. Lumbroso S; Lobaccaro JM; Vial C; Sassolas G; Ollagnon B; Belon C; Pouget J; Sultan C Horm Res; 1997; 47(1):23-9. PubMed ID: 9010714 [TBL] [Abstract][Full Text] [Related]
10. [X-chromosomal bulbospinal muscular atrophy (Kennedy syndrome)]. Berkhoff M; Sturzenegger M; Spiegel R; Rösler KM; Hess CW Schweiz Med Wochenschr; 1998 May; 128(21):817-23. PubMed ID: 9642748 [TBL] [Abstract][Full Text] [Related]
11. Kennedy's disease: a clinicopathologic correlation with mutations in the androgen receptor gene. Amato AA; Prior TW; Barohn RJ; Snyder P; Papp A; Mendell JR Neurology; 1993 Apr; 43(4):791-4. PubMed ID: 8469342 [TBL] [Abstract][Full Text] [Related]
12. 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]