Sertié, A L; Quimby, M; Moreira, E S; Murray, J; Zatz, Mayana 
; Antonarakis, S E; Passos-Bueno, Maria Rita
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
SERTIÉ, A L et al. A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3. Human Molecular Genetics, v. 5, n. 6, p. 843-847, 1996Tradução . . Disponível em: https://doi.org/10.1093/hmg/5.6.843. Acesso em: 05 nov. 2024.APA
Sertié, A. L., Quimby, M., Moreira, E. S., Murray, J., Zatz, M., Antonarakis, S. E., & Passos-Bueno, M. R. (1996). A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3. Human Molecular Genetics, 5( 6), 843-847. doi:10.1093/hmg/5.6.843NLM
Sertié AL, Quimby M, Moreira ES, Murray J, Zatz M, Antonarakis SE, Passos-Bueno MR. A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3 [Internet]. Human Molecular Genetics. 1996 ; 5( 6): 843-847.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1093/hmg/5.6.843Vancouver
Sertié AL, Quimby M, Moreira ES, Murray J, Zatz M, Antonarakis SE, Passos-Bueno MR. A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3 [Internet]. Human Molecular Genetics. 1996 ; 5( 6): 843-847.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1093/hmg/5.6.843
