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14. 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]
15. The expanded trinucleotide repeat in Kennedy's disease. Fischbeck KH Proc Assoc Am Physicians; 1995 Jul; 107(2):228-30. PubMed ID: 8624856 [No Abstract] [Full Text] [Related]
16. The DNA diagnosis for bulbospinal muscular atrophy. Ohno M; Yamada T; Kobayashi T; Goto I Clin Neurol Neurosurg; 1994 Feb; 96(1):20-3. PubMed ID: 8187377 [TBL] [Abstract][Full Text] [Related]
17. [X chromosome-linked bulbospinal neuronopathy in adults]. Mozolevskiĭ IuV Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(3):121-3. PubMed ID: 2728735 [TBL] [Abstract][Full Text] [Related]
18. [Familial distal progressive spinal amyotrophy with asymmetry of the lower limbs]. Nedelec C; Dubas F; Truelle JL; Pouplard F; Delestre F; Penisson-Besnier I Rev Neurol (Paris); 1987; 143(11):765-7. PubMed ID: 3432850 [TBL] [Abstract][Full Text] [Related]
19. [The DNA diagnosis of a familial case of Kennedy's spinal and bulbar amyotrophy]. Petrukhin AS; Zavadenko NN; Petrukhin AA; Evgrafov OV Zh Nevrol Psikhiatr Im S S Korsakova; 1997; 97(3):45-8. PubMed ID: 9157759 [TBL] [Abstract][Full Text] [Related]