Association between the p.V37I variant of GJB2 and hearing loss: a pedigree and meta-analysis
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PDF) The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals
The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals | PLOS ONE
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PDF) Mutational Analysis of GJB2 Gene in Non-Syndromic Hearing Loss from Patients at Children's Hospital 1- Ho Chi Minh City, Vietnam
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Genes | Free Full-Text | Haplotype Analysis of GJB2 Mutations: Founder Effect or Mutational Hot Spot? | HTML
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Evaluation of newborn screening bloodspot-based genetic testing as second tier screen for bedside newborn hearing screening - Genetics in Medicine
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