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Chromosomal Microarray Analysis in Fetuses with Growth Restriction and Normal Karyotype: A Systematic Review and Meta-Analysis
2017
Fetal Diagnosis and Therapy
Spain tion, Xp22.3 deletion, and 7q11.23 deletion (Williams-Beuren syndrome), particularly in isolated FGR. Conclusion: The use of genomic CMA provides a 4% incremental yield of detecting pathogenic CNVs in fetuses with isolated growth restriction and normal karyotype.
doi:10.1159/000479506
pmid:28889126
fatcat:cxvrgcavbfdrzkvbodyp2ncd5m