Molecular cytogenetic characterization of 16p11.2 microdeletions with diverse prenatal phenotypes: Four cases report and literature review

Objective: Chromosome 16p11.2 deletions have been recognized as a genetic disorder with well-described postnatal phenotypes. However, the prenatal manifestations are atypical for lacking of enough evidence. Case report: Four pregnant women underwent amniocentesis for cytogenetic analysis and chromos...

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主要な著者: Fagui Yue (著者), Qi Xi (著者), Xinyue Zhang (著者), Yuting Jiang (著者), Hongguo Zhang (著者), Ruizhi Liu (著者)
フォーマット: 図書
出版事項: Elsevier, 2022-05-01T00:00:00Z.
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