Cargando…
Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experience
BACKGROUND: Prenatal invasive genetic testing is commonly recommended to pregnancies of early-onset FGR or FGR combined with a structural defect. Our study aimed to explore the genetic findings for FGR without structural malformations according to cytogenetic karyotyping and single nucleotide polymo...
Autores principales: | Wu, Xiaoqing, He, Shuqiong, Li, Ying, Guo, Danhua, Chen, Xuemei, Liang, Bin, Wang, Meiying, Huang, Hailong, Xu, Liangpu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9878785/ https://www.ncbi.nlm.nih.gov/pubmed/36703098 http://dx.doi.org/10.1186/s12884-023-05394-y |
Ejemplares similares
-
Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype
por: Wu, Xiaoqing, et al.
Publicado: (2020) -
Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype
por: Su, Linjuan, et al.
Publicado: (2019) -
Copy number variations associated with fetal congenital kidney malformations
por: Cai, Meiying, et al.
Publicado: (2020) -
Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center
por: Cai, Meiying, et al.
Publicado: (2022) -
Performance of Chromosomal Microarray Analysis for Detection of Copy Number Variations in Fetal Echogenic Bowel
por: Fan, Xiangqun, et al.
Publicado: (2021)