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Publications by Emilia Vitale

Second Family With Hearing Impairment Linked to 19q13 and Refined DFNA4 Localisation

European Journal of Human Genetics

English

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Phenotypic Characterization of Hereditary Hearing Impairment Linked to DFNA25

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Y-Linked Inheritance of Non-Syndromic Hearing Impairment in a Large Chinese Family

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Genetic Basis of Y-Linked Hearing Impairment

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A Dutch Family With Hearing Loss Linked to the DFNA20/26 Locus

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A 4bp-Insertion in the Eya-Homologous Region (eyaHR) of EYA4 Causes Hearing Impairment in a Hungarian Family Linked to DFNA10

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The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research

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Childhood Hearing Impairment

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Mitochondrial tRNAIle A4317G Mutation May Be Associated With Hearing Impairment in a Han Chinese Family

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Newborn Hearing Screening vs Later Hearing Screening and Developmental Outcomes in Children With Permanent Childhood Hearing Impairment

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