Partial Trisomy 16p (16p12.2→pter) and Partial Monosomy 22q (22q13.31 →qter) Presenting With Fetal Ascites and Ventriculomegaly: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization
Objective: To present prenatal diagnosis and array comparative genomic hybridization (aCGH) characterization of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) presenting with fetal ascites and ventriculomegaly in the second trimester. Case Report: A 31-year-old woman, gr...
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Main Authors: | , , , , , , , , |
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Format: | Book |
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Elsevier,
2010-12-01T00:00:00Z.
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A1234.567 |
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Copy 1 | Available |