Figure 2From: CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX Haplotype analysis for pedigrees K at the (a) FEOM1 and (b) FEOM3 loci and BT at the (c) FEOM1 and (d) FEOM3 loci. Symbols are defined in the legend to figure 1. In each family the CFEOM1 phenotype is co-inherited with FEOM3 markers and not with FEOM1 markers.Back to article page