Fig. 1From: Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human geneGenealogy of the congenital cataract family. Solid symbols designate affected subjects. Slash indicates deceased individuals. The squares and circles indicate male and female, respectively; numbers inside diamonds indicate the number of siblings from a specific individual or coupleBack to article page