Fig. 1
From: Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1
Pedigree of the DYX5-linked family. Squares denote males and circles females. The 19 affected individuals marked with dots share the dyslexia susceptibility haplotype [11], and their DNA samples were pooled for sequencing on the Illumina platform. The DNA from the two affected individuals denoted by arrows was used in the CGI WGS. Circled dots indicate the individuals whose DNA samples were used in the Sanger sequencing of the exonic SNPs