Audiologic Phenotype and Progression in Pediatric STRC‐Related Autosomal Recessive Hearing Loss

Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approach

(2020) Bong Jik Kim et al.   GENETICS IN MEDICINE

STRC Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech Population

(2018) Simona Poisson Marková et al.   Genetic Testing and Molecular Biomarkers

STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic

(2017) Pavlina Plevova et al.   OTOLOGY & NEUROTOLOGY

Copy number variants are a common cause of non-syndromic hearing loss

(2014) A Shearer et al.   Genome Medicine

DFNB16 is a frequent cause of congenital hearing impairment: implementation ofSTRCmutation analysis in routine diagnostics

(2013) B. Vona et al.   CLINICAL GENETICS

Genetic testing for hearing loss in the United States should include deletion/duplication analysis for the deafness/infertility locus at 15q15.3

(2013) Nicole Hoppman et al.   Molecular Cytogenetics

Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment

(2011) Lauren J. Francey et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Audiologic Phenotype and Progression in GJB2 (Connexin 26) Hearing Loss

(2010) Margaret A. Kenna et al.   ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY

Connexin-26–associated deafness: Phenotypic variability and progression of hearing loss

(2010) Dylan K Chan et al.   GENETICS IN MEDICINE

Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane

(2010) Elisabeth Verpy et al.   JOURNAL OF COMPARATIVE NEUROLOGY

A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents

(2009) J Knijnenburg et al.   JOURNAL OF MEDICAL GENETICS