Genomic imbalances in syndromic congenital heart disease,
Abstract Objective: To identify pathogenic genomic imbalances in patients presenting congenital heart disease (CHD) with extra cardiac anomalies and exclusion of 22q11.2 deletion syndrome (22q11.2 DS). Methods: 78 patients negative for the 22q11.2 deletion, previously screened by fluorescence in sit...
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Main Authors: | , , , , , , , , , |
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Format: | Book |
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Elsevier.
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A1234.567 |
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