Rare copy number variants are common in young children with autism spectrum disorder
Acta Paediatrica2015Vol. 104(6), pp. 610–618
Citations Over TimeTop 12% of 2015 papers
Mats Eriksson, Agne Liedén, Joakim Westerlund, Anna Bremer, Josephine Wincent, Ellika Sahlin, Christopher Gillberg, Elisabeth Fernell, Britt‐Marie Anderlid
Abstract
Our results support the use of chromosomal microarray methods for the first tier genetic analysis of autism spectrum disorder. However, it is likely in the near future that chromosomal microarray methods will probably be replaced by whole-exome and whole-genome sequencing technologies in clinical genetic testing.
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