Figure 1 of Kloeckener-Gruissem, Mol Vis 2006; 12:350-355.

Figure 1. Pedigree of original Swiss family with dominantly inherited Wagner syndrome

Filled symbols represent affected individuals. Family members of generations III, IV, and V, who have been tested for the splice site mutation, are numbered. An arrow points to the index patient. Clinical information on the eye phenotype of generation I is not available.

(22 K)

Kloeckener-Gruissem, Mol Vis 2006; 12:350-355 <>
©2006 Molecular Vision <>
ISSN 1090-0535