Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality
Objective: We present prenatal diagnosis of familial transmission of 17q12 duplication associated with no apparent phenotypic abnormality. Case Report: A 36-year-old woman underwent amniocentesis at 17 weeks of gestation because of advanced maternal age. Cytogenetic analysis revealed a karyotype of...
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Main Authors: | , , , , , , , |
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Format: | Book |
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Elsevier,
2016-12-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
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A1234.567 |
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Copy 1 | Available |