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...
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Main Authors: | , , , , , , |
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Format: | Book |
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Elsevier,
2019-11-01T00:00:00Z.
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A1234.567 |
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