Microarray‐based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances
Objective: To identify chromosomal imbalances by whole‐genome microarray‐based comparative genomic hybridization (array‐CGH) in DNA samples of neonates with congenital anomalies of unknown cause from a birth defects monitoring program at a public maternity hospital. Methods: A blind genomic analysis...
Glavni autori: | , , , |
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Format: | Članak |
Jezik: | Portuguese |
Izdano: |
Brazilian Society of Pediatrics
2015-01-01
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Serija: | Jornal de Pediatria (Versão em Português) |
Teme: | |
Online pristup: | http://www.sciencedirect.com/science/article/pii/S2255553614001542 |