Figure 1
From: LINS, a modulator of the WNT signaling pathway, is involved in human cognition
Clinical Data of the studied family. A. Pedigree showing the mode of inheritance for an autosomal recessive intellectual disability phenotype in a consanguineous family from United Arab Emirates. The studied members are indicated by numbers and asterisks. B. Appearance of the 2 affected sibs, 1) II1 at age 8 years and 2) II2 at age 3 years. Note the flattening of the midface.