Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrum

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Title
Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrum
Authors
Keywords
Psychomotor delay, Intellectual disability, Autism spectrum disorder, 17q21.31 microduplication, Genetic syndrome, KANSL1
Journal
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
Volume 20, Issue 1, Pages 183-187
Publisher
Elsevier BV
Online
2015-10-25
DOI
10.1016/j.ejpn.2015.09.010

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