Fig. 1
From: Genomic and phenotypic delineation of congenital microcephaly
Pie chart showing the grouping and distribution of the variants identified in this cohort into four categories: variants in MCPH genes, variants in genes with established disease phenotypes in humans, variants in genes reported previously as candidate genes, and variants in genes with no established disease phenotypes in humans. MCPH, microcephaly primary hereditary.
