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Hearing, Balance and Communication Volume 11, 2013 - Issue 3: Hearing in early childhood
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Research Article

Genetic and clinical diagnosis in non-syndromic hearing loss

Manou SommenUniversity of Antwerp, Department of Medical Genetics, Antwerp, Belgium
,
Guy van CampUniversity of Antwerp, Department of Medical Genetics, Antwerp, BelgiumCorrespondence[email protected]
&
An BoudewynsUniversity of Antwerp, Department of Otorhinolaryngology, Head and Neck Surgery, Antwerp, Belgium
Pages 138-145 | Accepted 30 May 2013, Published online: 01 Aug 2013

Citations (5)

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Read on this site (1)

Manou Sommen, Wim Wuyts & Guy Van Camp. (2017) Molecular diagnostics for hereditary hearing loss in children. Expert Review of Molecular Diagnostics 17:8, pages 751-760.
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Articles from other publishers (4)

Wen Xie & Maoli Duan. 2022. Recent Advances in Audiological and Vestibular Research. Recent Advances in Audiological and Vestibular Research.
Friedrich Bootz. 2020. Pädiatrie. Pädiatrie 2987 2989 .
Friedrich Bootz. 2019. Pädiatrie. Pädiatrie 1 3 .
Manou Sommen, Isabelle Schrauwen, Geert Vandeweyer, Nele Boeckx, Jason J. Corneveaux, Jenneke van den Ende, An Boudewyns, Els De Leenheer, Sandra Janssens, Kathleen Claes, Margriet Verstreken, Nicola Strenzke, Friederike Predöhl, Wim Wuyts, Geert Mortier, Maria Bitner-Glindzicz, Tobias Moser, Paul Coucke, Matthew J. Huentelman & Guy Van Camp. (2016) DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System. Human Mutation 37:8, pages 812-819.
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