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Published in 2019 at "European Neuropsychopharmacology"
DOI: 10.1016/j.euroneuro.2017.08.087
Abstract: Background 3q29 Deletion Syndrome (3q29DS) is a rare (~1:30000) genomic disorder characterized by a 1.6 Mb deletion on chromosome 3, and is associated with developmental delay, intellectual disability, and a significantly increased risk for neuropsychiatric disorders,…
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Keywords:
prevalence asd;
diagnosis asd;
3q29 deletion;
deletion ... See more keywords