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Figure 1 | Orphanet Journal of Rare Diseases

Figure 1

From: Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study

Figure 1

Pedigrees of the seven families with hearing loss. Double horizontal bars above a symbol indicate individuals who underwent genetic analysis by targeted next-generation sequencing. Single horizontal bars above a symbol indicate individuals who underwent analysis by Sanger sequencing. A-G denote pedigrees of family 1-7, respectively.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172