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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フォーマット: | 図書 |
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Elsevier,
2022-05-01T00:00:00Z.
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請求記号: |
A1234.567 |
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所蔵 1 | 利用可 |