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P592: Cytogenetic and microarray analysis of prenatally detected congenital heart defects (CHD): Diagnostic findings and variation among CHD subtypes
oleh: Stuart Schwartz, Alexandra Arreola, Inder Gadi, Gloria Haskell, Bing Huang, Judith Knops, Andrea Penton, Karen Phillips
Format: | Article |
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Diterbitkan: | Elsevier 2024-01-01 |
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