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Case report

First published 2022-1

Cochlear implantation in a Chinese patient with a novel frameshift variant in POU3F4 gene and incomplete partition type III: a case report

Lanye Hu, Jie Chen, Ruen Yao [...]

Journal of International Medical Research

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Research article

First published 1997-4

Molecular Analysis of the Pou3F4 Gene in Patients with Clinical and Radiographic Evidence of X-Linked Mixed Deafness with Perilymphatic Gusher

Yelena Bykhovskaya, David F. Wilson, Rick A. Friedman [...]

Annals of Otology,Rhinology & Laryngology

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Research article

First published 2015-5

De Novo Mutation in X-Linked Hearing Loss–Associated POU3F4 in a Sporadic Case of Congenital Hearing Loss

Hideaki Moteki, A. Eliot Shearer, Shuji Izumi [...]

Annals of Otology,Rhinology & Laryngology

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Research article

First published 2019-06

Identification of a Novel Frameshift Variant of POU3F4 and Genetic Counseling of Korean Incomplete Partition Type III Subjects Based on Detailed Genotypes

Jeong Hun Jang, Jayoung Oh, Jin Hee Han [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2010-12

Cochlear Implantation in Children with Congenital X-Linked Deafness Due to Novel Mutations in POU3F4 Gene

Konstantina M. Stankovic, Ann Marie Hennessey, Barbara Herrmann [...]

Annals of Otology,Rhinology & Laryngology

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Case report

First published 2016-2

Positive Outcomes and Surgical Strategies for Bilateral Cochlear Implantation in a Child With X-Linked Deafness

Leslie Kim, C. Ellis Wisely, Shana Lucius [...]

Annals of Otology,Rhinology & Laryngology

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Research article

First published 2014-9

Positive Outcomes and Surgical Strategies for Bilateral Cochlear Implantation in a Child with X-Linked Deafness

Leslie Kim, Clayton E. Wisely, Shana Lucius [...]

Otolaryngology–Head and Neck Surgery

Search results

Cochlear implantation in a Chinese patient with a novel frameshift variant in POU3F4 gene and incomplete partition type III: a case report

Molecular Analysis of the Pou3F4 Gene in Patients with Clinical and Radiographic Evidence of X-Linked Mixed Deafness with Perilymphatic Gusher

De Novo Mutation in X-Linked Hearing Loss–Associated POU3F4 in a Sporadic Case of Congenital Hearing Loss

Identification of a Novel Frameshift Variant of POU3F4 and Genetic Counseling of Korean Incomplete Partition Type III Subjects Based on Detailed Genotypes

Cochlear Implantation in Children with Congenital X-Linked Deafness Due to Novel Mutations in POU3F4 Gene

Positive Outcomes and Surgical Strategies for Bilateral Cochlear Implantation in a Child With X-Linked Deafness

Positive Outcomes and Surgical Strategies for Bilateral Cochlear Implantation in a Child with X-Linked Deafness