Aoi, Hiromi; Mizuguchi, Takeshi; Ceroni, Jose Ricard; Kim, Veronica Eun Hue; Furquim, Isabel; Honjo, Rachel S; Iwaki, Takuma; Suzuki, Toshifumi; Sekiguchi, Futoshi; Kim, Chong Ae 
Fonte: Journal of human genetics. Unidade: FM
Assuntos: ANORMALIDADES MÚLTIPLAS, SEQUENCIAMENTO GENÉTICO, GENÔMICA, TRANSCRIÇÃO GÊNICA, REAÇÃO EM CADEIA POR POLIMERASE
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AOI, Hiromi et al. Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndrome. Journal of human genetics, v. 64, n. 10, p. 967-978, 2019Tradução . . Disponível em: https://doi.org/10.1038/s10038-019-0643-z. Acesso em: 04 nov. 2024.APA
Aoi, H., Mizuguchi, T., Ceroni, J. R., Kim, V. E. H., Furquim, I., Honjo, R. S., et al. (2019). Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndrome. Journal of human genetics, 64( 10), 967-978. doi:10.1038/s10038-019-0643-zNLM
Aoi H, Mizuguchi T, Ceroni JR, Kim VEH, Furquim I, Honjo RS, Iwaki T, Suzuki T, Sekiguchi F, Kim CA. Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndrome [Internet]. Journal of human genetics. 2019 ; 64( 10): 967-978.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/s10038-019-0643-zVancouver
Aoi H, Mizuguchi T, Ceroni JR, Kim VEH, Furquim I, Honjo RS, Iwaki T, Suzuki T, Sekiguchi F, Kim CA. Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndrome [Internet]. Journal of human genetics. 2019 ; 64( 10): 967-978.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/s10038-019-0643-z
