Source: Journal of Human Genetics. Unidade: IB
ABNT
LEZIROVITZ, Karina et al. Is autosomal recessive deafness associated with oculocutaneous albinism a "coincidence syndrome"?. Journal of Human Genetics, v. 51, p. 716-720, 2006Tradução . . Disponível em: https://doi.org/10.1007/s10038-006-0003-7. Acesso em: 27 abr. 2024.APA
Lezirovitz, K., Nicastro, F. S., Pardono, E., Abreu-Silva, R. S., Batissoco, A. C., Neustein, I., et al. (2006). Is autosomal recessive deafness associated with oculocutaneous albinism a "coincidence syndrome"? Journal of Human Genetics, 51, 716-720. doi:10.1007/s10038-006-0003-7NLM
Lezirovitz K, Nicastro FS, Pardono E, Abreu-Silva RS, Batissoco AC, Neustein I, Spinelli M, Mingroni Netto RC. Is autosomal recessive deafness associated with oculocutaneous albinism a "coincidence syndrome"? [Internet]. Journal of Human Genetics. 2006 ; 51 716-720.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1007/s10038-006-0003-7Vancouver
Lezirovitz K, Nicastro FS, Pardono E, Abreu-Silva RS, Batissoco AC, Neustein I, Spinelli M, Mingroni Netto RC. Is autosomal recessive deafness associated with oculocutaneous albinism a "coincidence syndrome"? [Internet]. Journal of Human Genetics. 2006 ; 51 716-720.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1007/s10038-006-0003-7