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. 2018 Jan 12;26(3):340–349. doi: 10.1038/s41431-017-0087-x

Fig. 1.

Fig. 1

Pedigrees of families in which Fryns syndrome segregates with homozygous PIGN loss of function alleles. The hatched shading for individual II: 2 of family 3 indicates a probably affected patient. PIGN genotype: +/+, wildtype; +/−, heterozygous variant or deletion; −/−, homozygous variant or deletion