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Publications by S. Manolidis

DNA Sequence Analysis and Genotype-Phenotype Assessment in 71 Patients With Syndromic Hearing Loss or Auditory Neuropathy

English

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Genotype-Phenotype Correlation Analysis of MYO15A Variants in Autosomal Recessive Non-Syndromic Hearing Loss

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Comprehensive Analysis of Syndromic Hearing Loss Patients in Japan

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Amelogenesis Imperfecta: Genotype-Phenotype Studies in 71 Families

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Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss

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GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss

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Electrophysiological Assessment of Auditory Processing Disorder in Children With Non-Syndromic Cleft Lip and/or Palate

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Which Patients With a Unilateral Hearing Aid for Symmetric Sensorineural Hearing Loss Have Auditory Deprivation?

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