Clinical Experience of Prenatal Chromosomal Microarray Analysis in 6159 Ultrasonically Abnormal Fetuses
Author:
Funder
Xi 'an City Innovation Ability strong base plan - medical research project
The National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynecology
Link
https://link.springer.com/content/pdf/10.1007/s43032-023-01399-2.pdf
Reference33 articles.
1. Mone F, McMullan DJ, Williams D, et al. Evidence to support the clinical utility of prenatal exome sequencing in evaluation of the fetus with congenital anomalies: scientific impact paper No. 64 [February] 2021. BJOG. 2021;128(9):e39–50. https://doi.org/10.1111/1471-0528.16616.
2. Hu T, Tian T, Zhang Z, et al. Prenatal chromosomal microarray analysis in 2466 fetuses with ultrasonographic soft markers: a prospective cohort study. Am J Obstet Gynecol. 2021;224(5):516. https://doi.org/10.1016/j.ajog.2020.10.039.
3. Hu ZM, Li LL, Zhang H, et al. Clinical application of chromosomal microarray analysis in pregnant women with advanced maternal age and fetuses with ultrasonographic soft markers. Med Sci Monit. 2021;27:e929074. https://doi.org/10.12659/MSM.929074.
4. American College of O and Gynecologists Committee on G. Committee Opinion No. 581: the use of chromosomal microarray analysis in prenatal diagnosis. Obstet Gynecol. 2013;122(6):1374–7. https://doi.org/10.1097/01.AOG.0000438962.16108.d1.
5. Miller DT, Adam MP, Aradhya S, et al. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet. 2010;86(5):749–64. https://doi.org/10.1016/j.ajhg.2010.04.006.
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