Source: Human Reproduction. Unidade: FMRP
Subjects: ABERRAÇÕES DOS CROMOSSOMOS SEXUAIS, ESTUDOS DE COORTES, RECÉM-NASCIDO, GRAVIDEZ, PREVALÊNCIA
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HUI, Lisa et al. A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort. Human Reproduction, v. 35, n. 3, p. 694-704, 2020Tradução . . Disponível em: https://doi.org/10.1093/humrep/dez286. Acesso em: 28 set. 2024.APA
Hui, L., Poulton, A., Kluckow, E., Lindquist, A., Hutchinson, B., Pertile, M. D., et al. (2020). A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort. Human Reproduction, 35( 3), 694-704. doi:10.1093/humrep/dez286NLM
Hui L, Poulton A, Kluckow E, Lindquist A, Hutchinson B, Pertile MD, Bonacquisto L, Gugasyan L, Kulkarni A, Costa FDS. A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort [Internet]. Human Reproduction. 2020 ; 35( 3): 694-704.[citado 2024 set. 28 ] Available from: https://doi.org/10.1093/humrep/dez286Vancouver
Hui L, Poulton A, Kluckow E, Lindquist A, Hutchinson B, Pertile MD, Bonacquisto L, Gugasyan L, Kulkarni A, Costa FDS. A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort [Internet]. Human Reproduction. 2020 ; 35( 3): 694-704.[citado 2024 set. 28 ] Available from: https://doi.org/10.1093/humrep/dez286