Associated Papers
Genetic analysis of 106 sporadic cases with hearing loss in the UAE population.
Tlili A et al.
Human Genomics, 2024
Next-generation sequencing for genetic testing of hearing loss populations.
Wang L et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2024
Follow-up of infants with mild-to-moderate sensorineural hearing loss over three years.
Hu Y et al.
International Journal of Pediatric Otorhinolaryngology, 2023
Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations.
Yu X et al.
Orphanet Journal of Rare Diseases, 2020
Diagnosis and Treatment of Congenital Sensorineural Hearing Loss.
Chari DA et al.
Current Otorhinolaryngology Reports, 2017
Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic.
Mehta D et al.
American Journal of Medical Genetics. Part A, 2016
The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations.
Yan D et al.
Genetic Testing and Molecular Biomarkers, 2015
Autosomal recessive nonsyndromic deafness genes: a review.
Duman D et al.
Frontiers in Bioscience (landmark Edition), 2012
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.
Mahdieh N et al.
Journal of Human Genetics, 2010
Genetics of congenital hearing impairment: a clinical approach.
Tranebaerg L
International Journal of Audiology, 2008
Non-syndromic, autosomal-recessive deafness.
Petersen MB et al.
Clinical Genetics, 2006
Hereditary deafness and phenotyping in humans.
Bitner-Glindzicz M
British Medical Bulletin, 2002
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