Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother

Objective: We present prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother. Case report: A 28-year-old woman primigravid underwent amniocentesis at 23 weeks of gestation because of fetal ultrasoun...

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Main Authors: Chih-Ping Chen (Author), Chen-Yu Chen (Author), Schu-Rern Chern (Author), Peih-Shan Wu (Author), Shin-Wen Chen (Author), Fang-Tzu Wu (Author), Wayseen Wang (Author)
Format: Book
Published: Elsevier, 2021-01-01T00:00:00Z.
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