Source: Human Genetics and Genomics Advances. Unidade: FMRP
Subjects: GENÉTICA APLICADA, MUTAÇÃO GENÉTICA, DELEÇÃO DE GENES, DOENÇAS GENÉTICAS, DOENÇAS RARAS
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ZHANG, Chaofan et al. Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability. Human Genetics and Genomics Advances, v. 3, n. 1, p. 1-19, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.xhgg.2021.100074. Acesso em: 09 fev. 2026.APA
Zhang, C., Jolly, A., Shayota, B. J., Mazzeu, J. F., Du, H., Dawood, M., et al. (2022). Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability. Human Genetics and Genomics Advances, 3( 1), 1-19. doi:10.1016/j.xhgg.2021.100074NLM
Zhang C, Jolly A, Shayota BJ, Mazzeu JF, Du H, Dawood M, Soper PC, Lima AR de, Ferreira BM, Coban-Akdemir Z, White J, Martelli LR. Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability [Internet]. Human Genetics and Genomics Advances. 2022 ; 3( 1): 1-19.[citado 2026 fev. 09 ] Available from: https://doi.org/10.1016/j.xhgg.2021.100074Vancouver
Zhang C, Jolly A, Shayota BJ, Mazzeu JF, Du H, Dawood M, Soper PC, Lima AR de, Ferreira BM, Coban-Akdemir Z, White J, Martelli LR. Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability [Internet]. Human Genetics and Genomics Advances. 2022 ; 3( 1): 1-19.[citado 2026 fev. 09 ] Available from: https://doi.org/10.1016/j.xhgg.2021.100074
