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Genomic imbalances in syndromic congenital heart disease

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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 situ hybridi...

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Main Authors: Miriam Coelho Molck (Author), Milena Simioni (Author), Társis Paiva Vieira (Author), Ilária Cristina Sgardioli (Author), Fabíola Paoli Monteiro (Author), Josiane Souza (Author), Agnes Cristina Fett‐Conte (Author), Têmis Maria Félix (Author), Isabella Lopes Monlléo (Author), Vera Lúcia Gil‐da‐Silva‐Lopes (Author)
Format: Book
Published: Brazilian Society of Pediatrics, 2017-09-01T00:00:00Z.
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