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Figure 1 | Orphanet Journal of Rare Diseases

Figure 1

From: Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families

Figure 1

Pedigree diagrams of 8 Korean families with autosomal dominant hearing loss. An asterisk in the upper right corner of the symbol indicates an individual whose genomic DNA was analyzed by targeted sequencing. Co-segregation of the candidate variations detected in the targeted sequencing and the phenotype of hearing loss was confirmed via Sanger sequencing of DNA from the individuals marked by a bar. Squares and circles represent males and females, respectively. Filled symbols represent affected individuals, and slashes indicate deceased individuals.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172