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Guy Van Camp
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Journal Articles

Genotype-Phenotype Correlation for DFNA22: Characterization of Non-Syndromic, Autosomal Dominant, Progressive Sensorineural Hearing Loss due to MYO6 Mutations

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Subject Area:
Audiology and Speech , Further Areas , Neurology and Neuroscience
Vedat Topsakal, Nele Hilgert, Joost van Dinther, Lisbeth Tranebjærg, Nanna D. Rendtorff, Andrzej Zarowski, Erwin Offeciers, Guy Van Camp, Paul van de Heyning
Journal: Audiology and Neurotology
Audiol Neurotol (2010) 15 (4): 211–220.
https://doi.org/10.1159/000255339
Published Online: 05 November 2009
View articletitled, Genotype-Phenotype Correlation for DFNA22: Characterization of Non-Syndromic, Autosomal Dominant, Progressive Sensorineural Hearing Loss due to MYO6 Mutations
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Journal Articles

Sex-Related Hearing Impairment in Wolfram Syndrome Patients Identified by Inactivating WFS1 Mutations

Available to Purchase
Subject Area:
Audiology and Speech , Further Areas , Neurology and Neuroscience
Ronald J.E. Pennings, Patrick L.M. Huygen, Jody M.W. van den Ouweland, Kim Cryns, Lambert D. Dikkeschei, Guy van Camp, Cor W.R.J. Cremers
Journal: Audiology and Neurotology
Audiol Neurotol (2004) 9 (1): 51–62.
https://doi.org/10.1159/000074187
Published Online: 19 December 2003
View articletitled, Sex-Related Hearing Impairment in Wolfram Syndrome Patients Identified by Inactivating WFS1 Mutations
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Journal Articles

Deafness Genes and Their Diagnostic Applications

Available to Purchase
Subject Area:
Audiology and Speech , Further Areas , Neurology and Neuroscience
Kim Cryns, Guy van Camp
Journal: Audiology and Neurotology
Audiol Neurotol (2004) 9 (1): 2–22.
https://doi.org/10.1159/000074183
Published Online: 19 December 2003
View articletitled, Deafness Genes and Their Diagnostic Applications
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