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    <identifier>10.57760/sciencedb.zhwcyxzz.00429</identifier>
    <datestamp>2025-10-20T11:12:26Z</datestamp>
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  <dc:date>2025-10-20</dc:date>
  <dc:title>Prenatal Diagnosis and Literature Review of fetuses with 1q21.1microdeletion/microduplication syndrome</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.zhwcyxzz.00429</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Objective To explore the clinical characteristics of fetuses with 1q21.1 microdeletion/microduplication, and to provide a basis for clinical consultation.</dc:description>
  <dc:subject>Chromosomal microarray analysis; 1q21.1 microdeletion syndrome; 1q21.1 microduplication syndrome; prenatal diagnosis; copy number variation</dc:subject>
  <dc:creator>Ting.LIU</dc:creator>
  <dc:creator>Fuyan.LIU</dc:creator>
  <dc:creator>null.HUXiaohang</dc:creator>
  <dc:creator>Aizhong.HAN</dc:creator>
  <dc:creator>Liqing.JIANG</dc:creator>
  <dc:creator>Yanxiang.BAI</dc:creator>
  <dc:creator>Huan.GUO</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
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  <dc:publisher>Science Data Bank</dc:publisher>
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