Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria

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Mendelian Disorder, Developmental Biology, Genetic Disorder +2

Connexin-26 mutations in sporadic and inherited sensorineural deafness

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Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

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A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment

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Hereditary Hearing Loss and its Syndromes

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Robert J. Gorlin, Genetics, Genetic Epidemiology +23