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Citation: H. Kunst et al., The phenotype of DFNA13/COL11A2: Nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment, AM J OTOL, 21(2), 2000, pp. 181-187

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Citation: Pj. Coucke et al., Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families, HUM MOL GEN, 8(7), 1999, pp. 1321-1328

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Citation: G. Van Camp et al., A gene for autosomal dominant hearing impairment (DFNA14) maps to a regionon chromosome 4p16.3 that does not overlap the DFNA6 locus, J MED GENET, 36(7), 1999, pp. 532-536

Authors: Kunst, H Marres, H Huygen, P Van Camp, G Joosten, F Cremers, C

Citation: H. Kunst et al., Autosomal dominant non-syndromal low-frequency sensorineural hearing impairment linked to chromosome 4p16 (DFNA14): Statistical analysis of hearing threshold in relation to age and evaluation of vestibule-ocular functions, AUDIOLOGY, 38(3), 1999, pp. 165-173