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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|September 10, 2005
Audiometric, vestibular, and genetic aspects of a DFNA9 family with a G88E COCH mutationMartijn H Kemperman, Els M R De Leenheer, Patrick L M Huygen, et al.
Human Mutation|January 29, 2008
Branchio-oto-renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BORDana J Orten, Stephanie M Fischer, Jessica L Sorensen, et al.
American Journal of Medical Genetics. Part A|July 12, 2005
Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3Arjan P M de Brouwer, Hendrikus P M Kunst, Alice Krebsova, et al.
The Annals of Otology, Rhinology & Laryngology. Supplement|April 20, 2006
Consensus statements on the BAHA system: where do we stand at present?Ad F M Snik, Emmanuel A M Mylanus, David W Proops, et al.
Human Mutation|September 5, 2003
Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric diseaseKim Cryns, Theru A Sivakumaran, Jody M W Van den Ouweland, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|September 10, 2005
Vestibular deterioration precedes hearing deterioration in the P51S COCH mutation (DFNA9): an analysis in 74 mutation carriersAnne M L C Bischoff, Patrick L M Huygen, Martijn H Kemperman, et al.
Human Genetics|June 29, 2004
Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)Mirjam W J Luijendijk, Erwin Van Wijk, Anne M L C Bischoff, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 13, 2011
SDHAF2 (PGL2-SDH5) and hereditary head and neck paragangliomaHenricus P M Kunst, Martijn H Rutten, Jan-Pieter de Mönnink, et al.
International Journal of Pediatric Otorhinolaryngology|January 20, 2005
Hearing impairment in Dutch patients with connexin 26 (GJB2) and connexin 30 (GJB6) mutationsRegie Lyn P Santos, Yurii S Aulchenko, Patrick L M Huygen, et al.
European Journal of Human Genetics : EJHG|June 26, 2008
Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancerRob W J Collin, Anne-Martine R de Heer, Jaap Oostrik, et al.
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