Outcomes of clinical examination and genetic testing of 500 individuals with hearing loss evaluated through a genetics of hearing loss clinic
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
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4. A genotype-phenotype correlation for GJB2 (connexin 26) deafness
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1. Full etiologic spectrum of pediatric severe to profound hearing loss of consecutive 119 cases;Scientific Reports;2022-07-19
2. Ubiquitously Expressed Proteins and Restricted Phenotypes: Exploring Cell-Specific Sensitivities to Impaired tRNA Charging;Trends in Genetics;2020-02
3. Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic;American Journal of Medical Genetics Part A;2016-08-02
4. Rare compound heterozygosity involving dominant and recessive mutations of GJB2 gene in an assortative mating hearing impaired Indian family;European Archives of Oto-Rhino-Laryngology;2016-08-01
5. Etiological approach in patients with unidentified hearing loss;International Journal of Pediatric Otorhinolaryngology;2015-02
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