Associated Papers
Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta-analysis.
Aliazami F et al.
International Journal of Pediatric Otorhinolaryngology, 2023
Targeted next-generation sequencing of deaf patients from Southwestern China.
Li Y et al.
Molecular Genetics & Genomic Medicine, 2021
Hearing Screening Combined with Target Gene Panel Testing Increased Etiological Diagnostic Yield in Deaf Children.
Xie L et al.
Neural Plasticity, 2021
Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population.
Wu CC et al.
Genes, 2019
Republished: Genetic investigations in childhood deafness.
Parker M et al.
Postgraduate Medical Journal, 2015
Genetic investigations in childhood deafness.
Parker M et al.
Archives of Disease in Childhood, 2015
Prevalence of p.V37I variant of GJB2 among Chinese infants with mild or moderate hearing loss.
Huang Y et al.
International Journal of Clinical and Experimental Medicine, 2015
Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment.
Yuan Y et al.
Plos One, 2012
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
Mahdieh N et al.
Journal of Human Genetics, 2010
Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound.
Schrijver I
The Journal of Molecular Diagnostics : Jmd, 2004
Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins.
Rabionet R et al.
Human Mutation, 2000
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