Source: American Journal of Medical Genetics. Unidade: IB
Subjects: SÍNDROME DE ANGELMAN, RETARDO MENTAL, DOENÇAS DO SISTEMA NERVOSO CENTRAL, DOENÇAS GENÉTICAS
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FRIDMAN, Cintia et al. Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene. American Journal of Medical Genetics, v. 119A, n. 2, p. 180-183, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.20105. Acesso em: 13 out. 2024.APA
Fridman, C., Hosomi, N., Varela, M. C., Souza, A. H., Fukai, K., & Celia Priszkulnik Koiffmann,. (2003). Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene. American Journal of Medical Genetics, 119A( 2), 180-183. doi:10.1002/ajmg.a.20105NLM
Fridman C, Hosomi N, Varela MC, Souza AH, Fukai K, Celia Priszkulnik Koiffmann. Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene [Internet]. American Journal of Medical Genetics. 2003 ; 119A( 2): 180-183.[citado 2024 out. 13 ] Available from: https://doi.org/10.1002/ajmg.a.20105Vancouver
Fridman C, Hosomi N, Varela MC, Souza AH, Fukai K, Celia Priszkulnik Koiffmann. Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene [Internet]. American Journal of Medical Genetics. 2003 ; 119A( 2): 180-183.[citado 2024 out. 13 ] Available from: https://doi.org/10.1002/ajmg.a.20105
