Fig. 1From: Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 genePedigree of the family with phenotypic heterogeneity associating H syndrome and RDD: H syndrome patients (III.3, III.11, III.14, and III.28), RDD patient (III.20)Back to article page