Sage Journals: Discover world-class research

Retricted access

Research article

First published 2010-08

Mutations in the Connexin 29 Gene Are Not a Major Cause of Nonsyndromic Hearing Impairment in India

Puppala Venkat Ramchander, Khirod Chandra Panda, Ashok Kumar Panda

Genetic Testing and Molecular Biomarkers

Open access

Case report

First published 2021-4

Genetic mutations in patients with nonsyndromic hearing impairment of minority and Han Chinese ethnicities in Qinghai,China

Shihong Duan, Yufen Guo, Xingjian Chen [...]

Journal of International Medical Research

Retricted access

Research article

First published 2014-12

New and Rare GJB2 Alleles in Patients with Nonsyndromic Sensorineural Hearing Impairment: A Genotype/Auditory Phenotype Correlation

Ilaria Stanghellini, Elisabetta Genovese, Silvia Palma [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 2012-04

Large-Scale Screening of Mitochondrial DNA Mutations Among Iranian Patients with Prelingual Nonsyndromic Hearing Impairment

Mostafa Montazer Zohour, Mohammad Amin Tabatabaiefar, Fatemeh Azadegan Dehkordi [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 1997-8

Collaborative Study of Nonsyndromic Hereditary Hearing Impairment Supported by the Ministry of Health and Welfare of Japan

Ken Kitamura, Tomoyuki Hoshino, Kunihiro Fukushima

Otolaryngology–Head and Neck Surgery

Retricted access

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

Retricted access

Research article

First published 2012-09

Novel Mutations Affecting the Secondary Structure of MT-RNR1 Gene: A Causal Relationship with Profound Nonsyndromic Hearing Impairment

Gunda Padma, Puppala Venkat Ramchander, Vijaya Udaya Nandur [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 2010-04

Easy,Rapid,and Cost-Effective Methods for Identifying Carriers of Recurrent GJB2 Mutations Causing Nonsyndromic Hearing Impairment in the Greek Population

Haris Kokotas, Maria Grigoriadou, Angeliki Hatzaki [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 2017-02

A Genomic and Protein–Protein Interaction Analyses of Nonsyndromic Hearing Impairment in Cameroon Using Targeted Genomic Enrichment and Massively Parallel Sequencing

Kamogelo Lebeko, Noluthando Manyisa, Emile R. Chimusa [...]

OMICS: A Journal of Integrative Biology

Retricted access

Research article

First published 2011-6

Phenotype Analysis of an Australian DFNA9 Family with the I109N COCH Mutation

Robert J. Pauw, Patrick L. M. Huygen, Gordon M. Colditz [...]

Annals of Otology,Rhinology & Laryngology

Search results