Prenatal phenotypes and pregnancy outcomes of fetuses with recurrent 1q21.1 microdeletions and microduplications

OBJECTIVE: Chromosomal 1q21.1 deletions and duplications are genomic disorders that are usually diagnosed postnatally. However, the genotype–phenotype correlations of 1q21.1 copy number variants (CNVs) during the prenatal period are still not clear. This study aimed to provide a systematic summary o...

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Detalles Bibliográficos
Autores principales: Yue, Fagui, Yang, Xiao, Jiang, Yuting, Li, Shibo, Liu, Ruizhi, Zhang, Hongguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484100/
https://www.ncbi.nlm.nih.gov/pubmed/37692779
http://dx.doi.org/10.3389/fmed.2023.1207891

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484100/
https://www.ncbi.nlm.nih.gov/pubmed/37692779
http://dx.doi.org/10.3389/fmed.2023.1207891

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