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Publications by ZONG-XIN WANG
Mitochondrial COI/tRNASer(UCN) G7444A Mutation May Be Associated With Aminoglycoside-Induced and Non-Syndromic Hearing Impairment
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Related publications
Mitochondrial tRNAIle A4317G Mutation May Be Associated With Hearing Impairment in a Han Chinese Family
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
DFNB1 Non-Syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes
Frontiers in Molecular Neuroscience
Molecular Neuroscience
Molecular Biology
Cellular
Medical Genetics: Advances in Brief: Mitochondrial Ribosomal RNA Mutation Associated With Both Antibiotic-Induced and Non-Syndromic Deafness
Journal of Medical Genetics
Genetics
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
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation
AUDIOLOGY JAPAN
Whole Mitochondrial Genome Screening in Maternally Inherited Non-Syndromic Hearing Impairment Using a Microarray Resequencing Mitochondrial DNA Chip
European Journal of Human Genetics
Genetics
Assessment of Aminoglycoside-Induced Hearing Impairment in Hospitalized Neonates by TEOAE
Indian Journal of Otolaryngology and Head and Neck Surgery
Otorhinolaryngology
Surgery
A Novel De Novo Mutation in CEACAM16 Associated With Postlingual Hearing Impairment
Molecular Syndromology
Genetics
WNT10A Polymorphism May Be a Risk Factor for Non-Syndromic Hypodontia
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
