Prenatal diagnosis of a familial 9p12 amplification inherited from a father carrier
Objective: We present prenatal diagnosis of a familial 9p12 amplification inherited from a father carrier. Case report: A 38-year-old, gravida 3, para 2, woman underwent amniocentesis at 17 weeks of gestation because of advanced maternal age. Amniocentesis revealed a heteromorphic variant of chromos...
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Main Authors: | , , , , , , , , , |
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Format: | Book |
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Elsevier,
2021-09-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
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A1234.567 |
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Copy 1 | Available |