Microarray‐based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances

Microarray‐based comparative genomic hybridization analysis in neonates with congenital anomalies: detection of chromosomal imbalances

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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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Bibliographic Details
Main Authors: Luiza Emy Dorfman, Júlio César L. Leite, Roberto Giugliani, Mariluce Riegel
Format: Article
Language:Portuguese
Published: Brazilian Society of Pediatrics 2015-01-01
Series:Jornal de Pediatria (Versão em Português)
Subjects:
Birth defects
Congenital anomalies
Newborn selective screening
Chromosomal abnormalities
Molecular cytogenetics
Array‐CGH
Online Access:http://www.sciencedirect.com/science/article/pii/S2255553614001542

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http://www.sciencedirect.com/science/article/pii/S2255553614001542

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