Genomic imbalances in syndromic congenital heart disease

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- (Author)
Format: Book
Published: Elsevier, 2017-09-01T00:00:00Z.
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