RBM10 and X-linked intellectual disability: More recently, during a screen of >400 index patients from families with X-linked intellectual disability (ID; Kalscheuer et al., manuscript in preparation), a deletion of 1292 nt (ChrX: 46929367–46930658 bp, UCSC genome browser hg18) in RBM10 were found in a German family (Fig 6A and Supporting Information Fig S6A).