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Fig. 2 | BMC Medical Genetics

Fig. 2

From: Phenotype prediction of Mohr-Tranebjaerg syndrome (MTS) by genetic analysis and initial auditory neuropathy

Fig. 2

Pedigree, audiological phenotype and gene variation of Family 2. a Pedigree of Family 2. The affected subject is coloured black, and the proband is indicated by an arrow. b Audiograms of the proband (III:6). c Normal DPOAE result of the proband. d Sequencing chromatograms of TIMM8A showing the deletion in affected individuals (lower panel) compared with normal controls (upper panel). L, left, blue; R, right, red

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BMC Medical Genetics

ISSN: 1471-2350

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