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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Main Authors: | , , , , , , , , , , |
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Format: | Book |
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Elsevier,
2021-03-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
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A1234.567 |
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