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Audiological Medicine Volume 1, 2003 - Issue 1
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Research Article

A Review of Progressive Phenotypes in Nonsyndromic Autosomal Dominant Hearing Impairment

RONALD JE PENNINGS Department of Otorhinolaryngology University Medical Centre St Radboud Nijmegen The NetherlandsCorrespondence[email protected]
,
PATRICK LM HUYGEN Department of Otorhinolaryngology University Medical Centre St Radboud Nijmegen The Netherlands
,
GUY VAN CAMP Department of Medical Genetics Universitaire Instellingen Antwerpen Antwerp Belgium
&
COR WRJ CREMERS Department of Otorhinolaryngology University Medical Centre St Radboud Nijmegen The Netherlands
Pages 47-55 | Published online: 11 Jul 2009

Citations (9)

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Read on this site (4)

Dafydd Stephens & Sophia E. Kramer. (2005) The impact of a family history of hearing problems on those with hearing difficulties themselves: an exploratory study El impacto de la historia familiar de problemas auditivos en quienes tienen problemas auditivos: un estudio exploratorio. International Journal of Audiology 44:4, pages 206-212.
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Ross RA Coles, Susan Hill, Cormac Macnamara, Ross RA Coles, Susan Hill, Cormac Macnamara & Nial Macnamara. (2005) Idiopathic Hearing Loss Mimicking Noise-induced Hearing Loss. Audiological Medicine 3:2, pages 116-120.
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Silvano Prosser & Alessandro Martini. (2005) Editorial. Audiological Medicine 3:3, pages 147-153.
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PATRICK LM HUYGEN, RONALD JE PENNINGS & COR WRJ CREMERS. (2003) Characterizing and Distinguishing Progressive Phenotypes in Nonsyndromic Autosomal Dominant Hearing Impairment. Audiological Medicine 1:1, pages 37-46.
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Articles from other publishers (5)

Yi Yuan, Denise Yan, Jeffrey Skidmore, Prem Chapagain, Xuezhong Liu & Shuman He. (2023) Responsiveness of the electrically stimulated cochlear nerve in patients with a missense variant in ACTG1: preliminary results. Frontiers in Audiology and Otology 1.
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Hans J. ten Donkelaar, Martin Lammens & Akira HoriHans J. ten Donkelaar, Bernd Fritzsch, Johannes R. M. Cruysberg, Ronald J. E. Pennings, Jeroen J. Smits & Martin Lammens. 2023. Clinical Neuroembryology. Clinical Neuroembryology 445 521 .
Hans J. ten Donkelaar, Martin Lammens & Akira HoriHans J. ten Donkelaar, Johannes R. M. Cruysberg, Ronald Pennings & Martin Lammens. 2014. Clinical Neuroembryology. Clinical Neuroembryology 321 370 .
Vedat Topsakal, Ronald J. E. Pennings, Heleen te Brinke, Ben Hamel, Patrick L. M. Huygen, Hannie Kremer & Cor W. R. J. Cremers. (2005) Phenotype Determination Guides Swift Genotyping of a DFNA2/KCNQ4 Family With a Hot Spot Mutation (W276S). Otology & Neurotology 26:1, pages 52-58.
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Tamar Ben-Yosef & Thomas B. Friedman. (2003) The genetic bases for syndromic and nonsyndromic deafness among Jews. Trends in Molecular Medicine 9:11, pages 496-502.
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