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Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
J Med Genet. 2009 Apr;46(4):242-8. doi: 10.1136/jmg.2008.059907. Epub 2008 Sep 19.
J Med Genet. 2009.
PMID: 18805830
Free PMC article.
A rare exonic NRXN3 deletion segregating with neurodevelopmental and neuropsychiatric conditions in a three-generation Chinese family.
Yuan H, Wang Q, Liu Y, Yang W, He Y, Gusella JF, Song J, Shen Y.
Yuan H, et al.
Am J Med Genet B Neuropsychiatr Genet. 2018 Sep;177(6):589-595. doi: 10.1002/ajmg.b.32673. Epub 2018 Aug 4.
Am J Med Genet B Neuropsychiatr Genet. 2018.
PMID: 30076746
Free PMC article.
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