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:English
Published: Elsevier 2015-02-01
Series:Jornal de Pediatria
Subjects:
Defeitos congênitos
Anomalias congênitas
Triagem seletiva de recém-nascidos
Anomalias cromossômicas
Citogenética molecular
CGH-array
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572015000100059&lng=en&tlng=en

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http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572015000100059&lng=en&tlng=en

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