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Publications by Shan Fang

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

Journal of Dermatology

English

Related publications

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

Journal of Medical Genetics

English

A Novel Homozygous Mutation of GJB2—A New Variant of Keratitis-Ichthyosis-Deafness Syndrome?

JAAD Case Reports

English

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

Otology and Neurotology

Otorhinolaryngology

Sensory Systems

English

KID Syndrome: Report of a Scandinavian Patient With Connexin‐26 Gene Mutation

Acta Dermato-Venereologica

English

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

European Journal of Human Genetics

English

Dental Treatments Under the General Anesthesia in a Child With Keratitis, Ichthyosis, and Deafness Syndrome

Case Reports in Dentistry

English

Cx26 Keratitis Ichthyosis Deafness Syndrome Mutations Trigger Alternative Splicing of Cx26 to Prevent Expression and Cause Toxicity in Vitro

Royal Society Open Science

Multidisciplinary

English

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

Journal of Medical Genetics

English

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

Genetics Research International

Molecular Biology

English