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Publications by Safarina G. Malik
Prevalence of the Mitochondrial DNA A1555G Mutation in Sensorineural Deafness Patients in Island Southeast Asia
Journal of Human Genetics
Genetics
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Frequency and Clinical Features of Patients With Sensorineural Hearing Loss Associated With the A3243G Mutation of the Mitochondrial DNA in Otorhinolaryngic Clinics
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The ND4 G11696A Mutation May Influence the Phenotypic Manifestation of the Deafness-Associated 12S rRNA A1555G Mutation in a Four-Generation Chinese Family
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Aging and Deafness. Long Term Observation of Sensorineural Deafness.
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Visual Impairment in Severe and Profound Sensorineural Deafness.
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Ectodermal Dysplasia-Sensorineural Deafness Syndrome
Mutation Spectrum of Common Deafness-Causing Genes in Patients With Non-Syndromic Deafness in the Xiamen Area, China
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Multidisciplinary