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Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individualsBIJLSMA, E. K; GIJSBERS, A. C. J; LOEYS, B et al.European journal of medical genetics. 2009, Vol 52, Num 2-3, pp 77-87, issn 1769-7212, 11 p.Article
