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Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.
J Neurodev Disord. 2016 Jun 14;8:24. doi: 10.1186/s11689-016-9157-6. eCollection 2016.
J Neurodev Disord. 2016.
PMID: 27307794
Free PMC article.
Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2.
Moralli D, Nudel R, Chan MT, Green CM, Volpi EV, Benítez-Burraco A, Newbury DF, García-Bellido P.
Moralli D, et al.
Mol Cytogenet. 2015 Jun 10;8:36. doi: 10.1186/s13039-015-0148-1. eCollection 2015.
Mol Cytogenet. 2015.
PMID: 26060509
Free PMC article.
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