Prenatal Diagnosis of Chromosome 16p11.2 Microdeletion

(1) Objective: To investigate the prenatal diagnosis and genetic counseling for 16p11.2 microdeletion syndrome and to evaluate its pregnancy outcome. (2) Methods: This study included 4968 pregnant women who selected invasive prenatal diagnoses from 1 January 2017 to 1 August 2022. These 4698 pregnan...

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Detalles Bibliográficos
Autores principales: Wang, You, Zhou, Hang, Fu, Fang, Cheng, Ken, Yu, Qiuxia, Huang, Ruibin, Lei, Tingying, Yang, Xin, Li, Dongzhi, Liao, Can
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778018/
https://www.ncbi.nlm.nih.gov/pubmed/36553582
http://dx.doi.org/10.3390/genes13122315

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778018/
https://www.ncbi.nlm.nih.gov/pubmed/36553582
http://dx.doi.org/10.3390/genes13122315

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