Chromosome microarray in Australia: A guide for paediatricians
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1754.2011.02081.x/fullpdf
Reference22 articles.
1. Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation;Rauch;Am. J. Med. Genet.,2006
2. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies;Miller;Am. J. Hum. Genet.,2010
3. Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies;Edelmann;Ann. N. Y. Acad. Sci.,2009
4. Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13 926 subjects;Shaw-Smith;Genet. Med.,2009
5. Medical genetics diagnostic evaluation of the child with global developmental delay or intellectual disability;Moeschler;Curr. Opin. Neurol.,2008
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