Association of schizophrenia and becker dystrophy ( bmd ): a susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain (1991)
- Authors:
- USP affiliated authors: GENTIL FILHO, VALENTIM - FM ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidades: FM; IB
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Source:
- Título do periódico: American Journal of Human Genetics
- Volume/Número/Paginação/Ano: v.49, n.4 suppl., p.364, oct. 1991
- Conference titles: International Congress of Human Genetics
-
ABNT
ZATZ, Mayana et al. Association of schizophrenia and becker dystrophy ( bmd ): a susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain. American Journal of Human Genetics. [S.l.]: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 16 abr. 2024. , 1991 -
APA
Zatz, M., Melo, M. S., Passos-Bueno, M. R., Valada Filho, H., Vieira Filho, A. H. G., Vainzof, M., et al. (1991). Association of schizophrenia and becker dystrophy ( bmd ): a susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain. American Journal of Human Genetics. Faculdade de Medicina, Universidade de São Paulo. -
NLM
Zatz M, Melo MS, Passos-Bueno MR, Valada Filho H, Vieira Filho AHG, Vainzof M, Rapaport D, Gentil Filho V. Association of schizophrenia and becker dystrophy ( bmd ): a susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 364.[citado 2024 abr. 16 ] -
Vancouver
Zatz M, Melo MS, Passos-Bueno MR, Valada Filho H, Vieira Filho AHG, Vainzof M, Rapaport D, Gentil Filho V. Association of schizophrenia and becker dystrophy ( bmd ): a susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 364.[citado 2024 abr. 16 ] - Cosegregation of schizophrenia with becker muscular dystrophy: susceptibility locus for schizophrenia at xp21 or an effect of the dystrophin gene in the brain?
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