Sage Journals: Discover world-class research

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Research article

First published 2016-08

Genetic Basis of Nonsyndromic Sensorineural Hearing Loss in the Sub-Saharan African Island Population of São Tomé and Príncipe: The Role of the DFNB1 Locus?

Cristina Caroça, Tiago Morim de Matos, Diogo Ribeiro [...]

OMICS: A Journal of Integrative Biology

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Research article

First published 2012-6

Screening of SLC26A4,FOXI1,KCNJ10,and GJB2 in Bilateral Deafness Patients with Inner Ear Malformation

Kaitian Chen, Xianren Wang, Liang Sun

Otolaryngology–Head and Neck Surgery

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Research article

First published 2012-11

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

Peter J. King, Xiaomei Ouyang, Lilin Du [...]

Otolaryngology–Head and Neck Surgery

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Research article

First published 2006-12

High Frequency of 35delG GJB2 Mutation and Absence of del( GJB6-D13S1830 ) in Greek Cypriot Patients with Nonsyndromic Hearing Loss

Vassos Neocleous, Andreas Aspris, Vasken Shahpenterian [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 1991-8

Familial Sensorineural Hearing Loss: A Correlative Study of Audiologic,Radiographic,and Vestibular Findings

Kenny H. Chan, Joseph M. R. Furman, Elizabeth A. Eelkema [...]

Annals of Otology,Rhinology & Laryngology

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Research article

First published 2010-08

Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population

F. Basak Cengiz, Duygu Duman, Aslı Sırmacı [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2009-10

Mutations in MYH9 Exons 1,16,26,and 30 Are Infrequently Found in Japanese Patients with Nonsyndromic Deafness

Shinji Kunishima, Tatsuo Matsunaga, Yoshimi Ito [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2022-5

Otitis Media and Hearing Loss in Patients With Nonsyndromic Craniosynostosis: A Multicenter Study

Jeewanjot S. Grewal, Jason E. Cohn, Jacob Burdett [...]

The Cleft Palate Craniofacial Journal

Open access

Case report

First published 2021-6

Cochlear Nerve Canal Stenosis: Association With MYH14 and MYH9 Genes

Wenqi Liang, Line Wang, Xinyu Song [...]

Ear,Nose & Throat Journal

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Research article

First published 2011-05

Mutation Screening of the GJA7 (Cx45) Gene in a Large International Series of Probands with Nonsyndromic Hearing Impairment

Xiao Mei Ouyang, Denise Yan, Idil Aslan [...]

Genetic Testing and Molecular Biomarkers

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