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Fig. 1 | BMC Medical Genetics

Fig. 1

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

Fig. 1

Pedigree and audiological phenotype of Family 1. a Pedigree of Family 1. The affected subject is coloured black, the proband is indicated by an arrow, and unaffected members with black spots indicate obligate carriers of the causative variation. b Audiograms of the proband (III:2) and his mother (II:4). c Normal DPOAE result of the proband. d Absence of ABR waves and present CM waves in the proband. L, Left, blue; R, Right, red

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BMC Medical Genetics

ISSN: 1471-2350

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