Sage Journals: Discover world-class research

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Research article

First published 2021-7

A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family

Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin K Esoh [...]

Experimental Biology and Medicine

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Research article

First published 2020-9

GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana

Samuel M Adadey, Kevin K Esoh, Osbourne Quaye [...]

Experimental Biology and Medicine

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Research article

First published 2004-06

GJB2 and GJB6 Mutations in 165 Danish Patients Showing Non-Syndromic Hearing Impairment

Karen Gr⊘nskov, Lars Allan Larsen, Nanna Dahl Rendtorff [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2021-1

Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment

Oluwafemi G Oluwole, Kevin K Esoh, Edmond Wonkam-Tingang [...]

Experimental Biology and Medicine

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Correction

First published 2021-11

Corrigendum to A novel variant in DXML2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family

Experimental Biology and Medicine

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Research article

First published 1997-6

Middle Ear Pressure and Dysfunction of the Labyrinth: Is There a Relationship?

Wolfgang Maier, Milo Fradis, Uwe Ross [...]

Annals of Otology,Rhinology & Laryngology

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Research article

First published 2018-6

Understanding activity participation among individuals with Wolfram syndrome

Emily Bumpus, Tamara Hershey, Tasha Doty [...]

British Journal of Occupational Therapy

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Research article

First published 2020-9

Templates and temporality: An investigation of rhythmic motor production in a young man with Down Syndrome and hearing impairment

Tracy Jeffery, Sandra Whiteside

Psychology of Music

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Other

First published 2011-8

Etiologic Diagnosis of Nonsyndromic Genetic Hearing Loss in Adult vs Pediatric Populations

Peter King, Simon I. Angeli, Xiaomei Ouyang [...]

Otolaryngology–Head and Neck Surgery

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Research article

First published 2008-06

Four USH2A Founder Mutations Underlie the Majority of Usher Syndrome Type 2 Cases among Non-Ashkenazi Jews

Noa Auslender, Dikla Bandah, Leah Rizel [...]

Genetic Testing and Molecular Biomarkers

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