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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| Principais autores: | , , , , , , , , , |
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| Formato: | Livro |
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Brazilian Society of Pediatrics,
2017-09-01T00:00:00Z.
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| Número de Chamada: |
A1234.567 |
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