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: Chun-Xiang Zhou (著者), Xiang-Yu Zhu (著者), Yu-Jie Zhu (著者), Lei-Lei Gu (著者), Lin-Lin He (著者), Wei Liu (著者), Ying Yang (著者), Xing Wu (著者), Hong-Lei Duan (著者), Tong Ru (著者), Jie Li (著者)
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出版事項: Elsevier, 2021-03-01T00:00:00Z.
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