Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects
Objective: We present a familial 21q22.3 microduplication in a fetus associated with prenatally detected congenital heart defects (CHD). Case report: A 38-year-old woman underwent amniocentesis at 22 weeks of gestation because of sonographic findings of double outlet of right ventricle, ventricular...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2019-11-01
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| Series: | Taiwanese Journal of Obstetrics & Gynecology |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S1028455919302311 |