Fig. 1From: A rare case of a male child with post-zygotic de novo mosaic variant c.538C > T in MECP2 gene: a case report of Rett syndromePedigree chart of present case (1A). Affected individual is shaded in grey stripes. Unilateral right pre-axial polydactyly (1B). IGV depicts the causative variant in only 32% of the reads (1C) and Sanger sequencing chromatograms of the proband and his parents (1D)Back to article page