Prenatal and postnatal chromosomal microarray analysis in 885 cases of various congenital heart defects
Author:
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynecology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00404-021-06366-3.pdf
Reference40 articles.
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2. Committee on Genetics and the Society for Maternal-Fetal Medicine, Vora NL, Romero ST, Ralston SJ, Dugoff L, Kuller JA (2016) Committee opinion no. 682: microarrays and next-generation sequencing technology: the use of advanced genetic diagnostic tools in obstetrics and gynecology. Obstetr Gynecol 128(6):e262–e268
3. Shaffer LG, Rosenfeld JA, Dabell MP, Coppinger J, Bandholz AM, Ellison JW et al (2012) Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound. Prenat Diagn 32(10):986–995
4. Mademont-Soler I, Morales C, Soler A, Martínez-Crespo JM, Shen Y, Margarit E et al (2013) Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis. Ultrasound Obstetr Gynecol 41(4):375–382
5. Yan Y, Wu Q, Zhang L, Wang X, Dan S, Deng D et al (2014) Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease. Ultrasound Obstetr Gynecol 43(4):404–412
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