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Publications by Kay W Chang
Connexin-26–associated Deafness: Phenotypic Variability and Progression of Hearing Loss
Genetics in Medicine
Medicine
Genetics
Related publications
Screening of Connexin 26 in Nonsyndromic Hearing Loss
International Archives of Otorhinolaryngology
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Mutations of the Connexin 26 Gene in Families With Non-Syndromic Hearing Loss
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Sudden Deafness With Further Progression of Hearing Loss After Initial Examination.
Practica Otologica
Otorhinolaryngology
Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss
International Journal of Human Genetics
Genetics
Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss
International Journal of Human Genetics
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Connexin 26 (GJB2) Gene-Related Deafness and Speech Intelligibility After Cochlear Implantation
Otology and Neurotology
Medicine
Otorhinolaryngology
Sensory Systems
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Is Assortative Mating the Cause for the High Frequency of Connexin 26 (Cx 26) Deafness?
Genetics in Medicine
Medicine
Genetics
Recurrent Mutations in the Deafness Gene GJB2 (Connexin 26) in British Asian Families
Journal of Medical Genetics
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Blood Pressure Variability Is Associated With Hearing and Hearing Loss: A Population-Based Study in Males
International Journal of Hypertension
Internal Medicine