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. Author manuscript; available in PMC: 2012 May 1.
Published in final edited form as: Am J Med Genet A. 2011 Apr 11;155(5):1202–1211. doi: 10.1002/ajmg.a.33209

Figure 2.

Figure 2

Figure 2

Figure 2

Figure 2

Figure 2 A. Pedigrees of two families, L-1301 (upper pedigree) and L-3057 (lower pedigree) with hearing loss caused by a novel mutation in GJB2, D46N. The proband of each family is indicated by an arrow. All individuals who did not have audiograms are indicated with an asterisk. Studied branches are shown with capital letters. Figure 2 B. All genotypes are indicated on pedigrees beneath the studied individuals.