Molecular cytogenetic characterization of de novo concomitant proximal 21q deletion of 21q11.2q21.3 and distal Xp deletion of Xp22.33p22.2 due to an unbalanced X;21 translocation detected by amniocentesis
Objective: We present molecular cytogenetic characterization of de novo concomitant proximal 21q deletion of 21q11.2q21.3 and distal Xp deletion of Xp22.33p22.2 due to an unbalanced X; 21 translocation detected by amniocentesis. Case report: A 35-year-old, primigravid woman underwent amniocentesis a...
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Elsevier,
2023-01-01T00:00:00Z.
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A1234.567 |
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所蔵 1 | 利用可 |