Fig 1
From: High-resolution genomic microarrays for X-linked mental retardation
Overview of causative aberrations found by array CGH in patients with XLMR. A, All seven regions described so far with causative copy number variations resulting in XLMR, positioned on the X chromosome. Each locus is involved in a single case, except for region 7, encompassing MECP2, which has been found in 18 independent cases (see also Table 1 for further details). B–E, Detailed overviews for four submicroscopic aberrations in which a known XLMR gene is located (A, region 2 in B, 5 in D and 7 in E, respectively) or led to the identification of a novel XLMR gene (A, region 3 in C).
