Source: The Journal of Pediatrics. Unidades: IB, FM
Subjects: GENÉTICA MÉDICA, DELEÇÃO DE GENES, ANORMALIDADES CONGÊNITAS, DOENÇAS RARAS
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MONTENEGRO, Marilia Moreira et al. Expanding the phenotype of 8p23.1 Deletion Syndrome: eight new cases resembling the clinical spectrum of 22q11.2 microdeletion. The Journal of Pediatrics, v. 252, n. Ja 2023, p. 56-60, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jpeds.2022.08.051. Acesso em: 26 ago. 2024.APA
Montenegro, M. M., Camilotti, D., Quaio, R. D. 'angioli C., Gasparini, Y., Zanardo, E. A., Rangel-Santos, A., et al. (2023). Expanding the phenotype of 8p23.1 Deletion Syndrome: eight new cases resembling the clinical spectrum of 22q11.2 microdeletion. The Journal of Pediatrics, 252( Ja 2023), 56-60. doi:10.1016/j.jpeds.2022.08.051NLM
Montenegro MM, Camilotti D, Quaio RD'angioli C, Gasparini Y, Zanardo EA, Rangel-Santos A, Novo-Filho GM, Francisco G, Liro L, Nascimento AM, Chehimi SN, Soares DCQ, Krepischi ACV, Grassi MS, Honjo RS, Palmeira P, Kim CA, Carneiro-Sampaio MMS, Rosenberg C, Kulikowski LD. Expanding the phenotype of 8p23.1 Deletion Syndrome: eight new cases resembling the clinical spectrum of 22q11.2 microdeletion [Internet]. The Journal of Pediatrics. 2023 ; 252( Ja 2023): 56-60.[citado 2024 ago. 26 ] Available from: https://doi.org/10.1016/j.jpeds.2022.08.051Vancouver
Montenegro MM, Camilotti D, Quaio RD'angioli C, Gasparini Y, Zanardo EA, Rangel-Santos A, Novo-Filho GM, Francisco G, Liro L, Nascimento AM, Chehimi SN, Soares DCQ, Krepischi ACV, Grassi MS, Honjo RS, Palmeira P, Kim CA, Carneiro-Sampaio MMS, Rosenberg C, Kulikowski LD. Expanding the phenotype of 8p23.1 Deletion Syndrome: eight new cases resembling the clinical spectrum of 22q11.2 microdeletion [Internet]. The Journal of Pediatrics. 2023 ; 252( Ja 2023): 56-60.[citado 2024 ago. 26 ] Available from: https://doi.org/10.1016/j.jpeds.2022.08.051