Audiologic presentation of enlargement of the vestibular aqueduct according to theSLC26A4genotypes

Mutation spectrum and genotype–phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study

(2014) Maiko Miyagawa et al.   JOURNAL OF HUMAN GENETICS

Correlation between genotype and phenotype in patients with bi-allelicSLC26A4mutations

(2013) H.J. Lee et al.   CLINICAL GENETICS

SLC26A4 Genotypes and Phenotypes Associated with Enlargement of the Vestibular Aqueduct

(2011) Taku Ito et al.   CELLULAR PHYSIOLOGY AND BIOCHEMISTRY

Mutations of KCNJ10 Together with Mutations of SLC26A4 Cause Digenic Nonsyndromic Hearing Loss Associated with Enlarged Vestibular Aqueduct Syndrome

(2009) Tao Yang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Evaluation of the Thyroid in Patients With Hearing Loss and Enlarged Vestibular Aqueducts

(2009) Anne C. Madeo et al.   ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY

Phenotypic Analyses and Mutation Screening of the SLC26A4 and FOXI1 Genes in 101 Taiwanese Families with Bilateral Nonsyndromic Enlarged Vestibular Aqueduct (DFNB4) or Pendred Syndrome

(2009) Chen-Chi Wu et al.   AUDIOLOGY AND NEURO-OTOLOGY

Efficient Molecular Genetic Diagnosis of Enlarged Vestibular Aqueducts in East Asians

(2009) Byung Yoon Choi et al.   Genetic Testing and Molecular Biomarkers

Hypo-FunctionalSLC26A4variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype-phenotype correlation or coincidental polymorphisms?

(2009) Byung Yoon Choi et al.   HUMAN MUTATION

Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes

(2009) B Y Choi et al.   JOURNAL OF MEDICAL GENETICS

Mutation Analysis of Slc26a4 in Mainland Chinese Patients with Enlarged Vestibular Aqueduct

(2009) Samuel Reyes et al.   OTOLARYNGOLOGY-HEAD AND NECK SURGERY