16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders
16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders
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London: Nature Publishing Group UK
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Language
English
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Publisher
London: Nature Publishing Group UK
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Contents
The chromosome 16p13.11 heterozygous deletion is associated with a diverse array of neuropsychiatric disorders including intellectual disabilities, autism, schizophrenia, epilepsy and attention-deficit hyperactivity disorder. However the clinical significance of its reciprocal duplication is not clearly defined yet. We evaluated 1645 consecutive pe...
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Full title
16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders
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TN_cdi_proquest_miscellaneous_879106285
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_879106285
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ISSN
1434-5161
E-ISSN
1435-232X
DOI
10.1038/jhg.2011.42
