Source: Nature Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
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ROBIN, N H et al. Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2. Nature Genetics, v. 11, n. 4, p. 459-61, 1995Tradução . . Disponível em: https://doi.org/10.1038/ng1295-459. Acesso em: 27 abr. 2024.APA
Robin, N. H., Feldman, G. J., Aronson, A. L., Mitchell, H. F., Weksberg, R., Leonard, C. O., et al. (1995). Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2. Nature Genetics, 11( 4), 459-61. doi:10.1038/ng1295-459NLM
Robin NH, Feldman GJ, Aronson AL, Mitchell HF, Weksberg R, Leonard CO, Burton BK, Josephson KD, Laxova R, Aleck KA, Allanson JE. Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2 [Internet]. Nature Genetics. 1995 ;11( 4): 459-61.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1038/ng1295-459Vancouver
Robin NH, Feldman GJ, Aronson AL, Mitchell HF, Weksberg R, Leonard CO, Burton BK, Josephson KD, Laxova R, Aleck KA, Allanson JE. Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2 [Internet]. Nature Genetics. 1995 ;11( 4): 459-61.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1038/ng1295-459
