Characterization of autosomal dominant non-syndromic hearing loss loci

DFNA 4, 6, 10 and 13.

W. T. McGuirt, M. M. Lesperance, E. R. Wilcox, Hung Chih Chen, G. Van Camp, R. J. Smith

Research output: Contribution to journalReview article

3 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)84-96
Number of pages13
JournalAdvances in Oto-Rhino-Laryngology
Volume56
StatePublished - Jan 1 2000

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Dominant Genes
Genetic Linkage
Sensorineural Hearing Loss
Chromosome Mapping
Human Chromosomes
Genetic Markers
Hearing Loss

ASJC Scopus subject areas

  • Otorhinolaryngology

Cite this

McGuirt, W. T., Lesperance, M. M., Wilcox, E. R., Chen, H. C., Van Camp, G., & Smith, R. J. (2000). Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13. Advances in Oto-Rhino-Laryngology, 56, 84-96.

Characterization of autosomal dominant non-syndromic hearing loss loci : DFNA 4, 6, 10 and 13. / McGuirt, W. T.; Lesperance, M. M.; Wilcox, E. R.; Chen, Hung Chih; Van Camp, G.; Smith, R. J.

In: Advances in Oto-Rhino-Laryngology, Vol. 56, 01.01.2000, p. 84-96.

Research output: Contribution to journalReview article

McGuirt, WT, Lesperance, MM, Wilcox, ER, Chen, HC, Van Camp, G & Smith, RJ 2000, 'Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13.', Advances in Oto-Rhino-Laryngology, vol. 56, pp. 84-96.
McGuirt WT, Lesperance MM, Wilcox ER, Chen HC, Van Camp G, Smith RJ. Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13. Advances in Oto-Rhino-Laryngology. 2000 Jan 1;56:84-96.
McGuirt, W. T. ; Lesperance, M. M. ; Wilcox, E. R. ; Chen, Hung Chih ; Van Camp, G. ; Smith, R. J. / Characterization of autosomal dominant non-syndromic hearing loss loci : DFNA 4, 6, 10 and 13. In: Advances in Oto-Rhino-Laryngology. 2000 ; Vol. 56. pp. 84-96.
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