Publication | Closed Access
A novel X‐linked disorder with developmental delay and autistic features
72
Citations
42
References
2011
Year
Xq12-q13.3 duplication is a novel global developmental delay and autism-predisposing chromosomal aberration; pathogenesis of which may be mediated by increased dosage of genes contained in the duplication, including NLGN3, OPHN1, AR, EFNB1, TAF1, GJB1, and MED12.
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