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