Fig. 1
From: A novel mutation in TRIOBP gene leading to congenital deafness in a Chinese family
Identification of the individuals with hearing impairment. a. Pedigree analyses to identify the family members with hearing loss. The proband is indicated by an arrow. Genotypes are indicated as heterozygous 1342C > T (Heter1342C > T) for III34 and III45, and homozygous 1342C > T (Homo1342C > T) for (IV1 and IV2). b. Pure-tone audiograms to identify the hearing affected individuals. The individuals (IV1 and IV2) show severe to profound symmetric hearing impairment