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...

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Bibliografski detalji
Glavni autori: Luiza Emy Dorfman, Júlio César L. Leite, Roberto Giugliani, Mariluce Riegel
Format: Članak
Jezik:Portuguese
Izdano: Brazilian Society of Pediatrics 2015-01-01
Serija:Jornal de Pediatria (Versão em Português)
Teme:
Online pristup:http://www.sciencedirect.com/science/article/pii/S2255553614001542