Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series
Objective: To present the experience on prenatal features of 17q12 microdeletion and microduplication syndromes. Materials and methods: Prenatal chromosomal microarray analysis (CMA) were conducted between January 2015 and December 2018 at a single Chinese tertiary medical centre. Information of cas...
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主要な著者: | , , , , , , , , , , |
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フォーマット: | 図書 |
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Elsevier,
2021-03-01T00:00:00Z.
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請求記号: |
A1234.567 |
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所蔵 1 | 利用可 |