Fig. 2
From: Genomic imbalances defining novel intellectual disability associated loci
Overview of some patients with likely pathogenic duplications. a Patient C16 - facial appearance: mildly dysmorphic, with high forehead and frontal bossing, thick eyebrows and mildly anteverted nares; pedigree, schematic representation of the duplicated 1p region and expression pattern for genes FAM69A, DPYD and TGFBR3. b Patient R21 - facial appearance: large forehead, sparse lateral eyebrows, epicanthal folds, large nose, anteverted nares, long smooth philtrum, downturned corners of mouth and micrognathia; pedigree, schematic representation of the triplicated 9q region and expression pattern for genes FBXW2, NEK6 and PSMB7. c Patient R22 - facial appearance: mildly dysmorphic with large forehead and frontal central hair whorl; pedigree, schematic representation of the duplicated Xq region and expression pattern for CUL4B and LAMP2 genes. d Patient C20 - facial appearance: mildly dysmorphic patient with thick eyebrows, wide palpebral fissures and thin upper lip; pedigree and schematic representation of the duplicated Xq region. B2M and PPIB were used as housekeeping genes; * p < 0.05 (Student t-test)