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Microarray analysis in fetuses with duodenal obstruction: It is not just trisomy 21.

Wenwen ZhangTing-Ying LeiFang FuQiong DengRu LiDan WangXin YangDongzhi LiLiao Can
Published in: Prenatal diagnosis (2021)
Our cohort study demonstrated the value of CMA in fetuses with DO, suggesting that CNVs may underly genetic etiologies that should be considered in the diagnostic evaluation of DO. We think CMA should be recommended in case of DO.
Keyphrases
  • gestational age
  • genome wide
  • gene expression
  • dna methylation
  • preterm birth