Figure 2From: Mutations in zinc finger 407 [ZNF407] cause a unique autosomal recessive cognitive impairment syndromePedigree of the family segregating for the ZNF407 c.C5054G/p.S1685W mutation. Genotypes are indicated. Consanguinity line represents first cousin marriage. Two early miscarriages are not shown. Half shaded blocks indicate genotypes only. Full shaded blocks indicate both genotypes and phenotypes for the affected individuals.Back to article page