Fig. 1: A consanguineous family, PKCC212, with three members having cataracts. | Human Genome Variation

Fig. 1: A consanguineous family, PKCC212, with three members having cataracts.

From: A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts

Fig. 1

a Pedigree drawing of PKCC212 with the haplotypes of alleles for chromosome 22q microsatellite markers. Alleles forming the risk haplotype are shaded black, and alleles not cosegregating with arCC are shown in white. Square: male; circle: female; filled symbol: affected individual; the double line between individuals: consanguineous marriage; diagonal line through a symbol: deceased. b Slit-lamp photograph of affected individual V:3 in the PKCC212 showing nuclear cataracts.

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