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Publications by S. Rickard

Recurrent Mutations in the Deafness Gene GJB2 (Connexin 26) in British Asian Families

Journal of Medical Genetics

English

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Connexin 26 (GJB2) Gene-Related Deafness and Speech Intelligibility After Cochlear Implantation

Otology and Neurotology

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Mutations of Connexin 26 (GJB2) Gene in a Chinese Keratitis-Ichthyosis-Deafness Syndrome Patient With Squamous Cell Carcinoma

Journal of Dermatology

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Mutations of the Connexin 26 Gene in Families With Non-Syndromic Hearing Loss

Molecular Medicine Reports

Molecular Biology

Cancer Research

Molecular Medicine

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Mutations of Cx26 Gene (GJB2) for Prelingual Deafness in Taiwan

European Journal of Human Genetics

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A Common Founder for the 35delG GJB2 Gene Mutation in Connexin 26 Hearing Impairment

Journal of Medical Genetics

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Frequency of C.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients With Nonsyndromic Hearing Impairment

Genetics Research International

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Screening British CADASIL Families for Mutations in the NOTCH3 Gene

Journal of Medical Genetics

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Rapid Detection of the 35delG Mutation in the GJB2 Gene in Childhood Deafness

Journal of Medical Screening

Occupational Health

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Is Assortative Mating the Cause for the High Frequency of Connexin 26 (Cx 26) Deafness?

Genetics in Medicine

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