Molecular cytogenetic characterization of 2q deletion and Xq duplication associated with nasal bone dysplasia in prenatal diagnosis: A case report and literature review
Objective: We report a prenatal case of male fetus with a 2q13 deletion and an Xq27.3q28 duplication, presenting nasal bone dysplasia by ultrasound examination. And we compare the similarities of clinical features of cases consisting of similar 2q deletion and Xq duplication. Case report: A 30-year-...
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Main Authors: | , , , , , , |
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Format: | Book |
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Elsevier,
2022-01-01T00:00:00Z.
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Internet
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A1234.567 |
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