Fig. 3From: CMA analysis identifies homozygous deletion of MCPH1 in 2 brothers with primary Microcephaly-1Chromosome microarray analysis. Chromosome 8 with deletion at 8p23.2p23.1 is shown along the right side of the image. SNP-array results show the copy number state (black pedigree labels), weighted log2 ratio (green pedigree labels), and allele peaks (red pedigree labels) for proband (V.8), his brother (V.6), his mother (IV.6), his father (IV.7), and the MCPH1 gene at the deleted regionBack to article page