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2018

N Kalnak, S Stamouli, M Peyrard-Janvid, I Rabkina, M Becker, T Klingberg, J Kere, H Forssberg, K Tammimies

Enrichment of rare copy number variation in children with developmental language disorder Journal Article

Clinical Genetics, 94 (3-4), pp. 313–320, 2018, ISSN: 00099163.

Abstract | Links | Tags: 16p11.2 deletion syndrome, copy number variation, developmental language disorder, genetic testing