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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| Principais autores: | , , , , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Elsevier
2021-03-01
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| 叢編: | Taiwanese Journal of Obstetrics & Gynecology |
| 主題: | |
| 在線閱讀: | http://www.sciencedirect.com/science/article/pii/S1028455921000012 |
| 標簽: |
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