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Publications by Wafaa Shehata-Dieler
A Novel De Novo Mutation in CEACAM16 Associated With Postlingual Hearing Impairment
Molecular Syndromology
Genetics
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A Novel Splice-Site Mutation in the GJB2 Gene Causing Mild Postlingual Hearing Impairment
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A Novel Mutation in the WFS1gene Identified in a Taiwanese Family With Low-Frequency Hearing Impairment
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Mitochondrial tRNAIle A4317G Mutation May Be Associated With Hearing Impairment in a Han Chinese Family
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A Novel De Novo Dominant Mutation inISCUassociated With Mitochondrial Myopathy
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Risk Factor Associated With Hearing Impairment in Neonates
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Novel Missense Mutations in MYO7A Underlying Postlingual High- Or Low-Frequency Non-Syndromic Hearing Impairment in Two Large Families From China
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The Mitochondrial Transfer RNAAsp A7551G Mutation May Contribute to the Clinical Expression of Deafness Associated With the A1555G Mutation in a Pedigree With Hearing Impairment
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Impairment of Mitochondrial tRNAIle Processing by a Novel Mutation Associated With Chronic Progressive External Ophthalmoplegia
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Chronic Myeloid Leukemia Associated With Impairment of Hearing.
BMJ
