Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Tayfun Kirazli
Comprehensive Analysis of Deafness Genes in Families With Autosomal Recessive Nonsyndromic Hearing Loss
PLoS ONE
Multidisciplinary
Lemierre's Syndrome Case Secondary to Otitis Media
Turk Otolarengoloji Arsivi/Turkish Archives of Otolaryngology
Related publications
CORRIGENDUM: Comprehensive Analysis via Exome Sequencing Uncovers Genetic Etiology in Autosomal Recessive Nonsyndromic Deafness in a Large Multiethnic Cohort
Genetics in Medicine
Medicine
Genetics
A NovelESRRBDeletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment Among Pakistani Families
Genetics Research International
Genetics
Molecular Biology
Histopathology of Nonsyndromic Autosomal Dominant Midfrequency Sensorineural Hearing Loss
Otology and Neurotology
Medicine
Otorhinolaryngology
Sensory Systems
Neurology
Mapping of a Novel Autosomal Recessive Nonsyndromic Deafness Locus (DFNB46) to Chromosome 18p11.32-P11.31
American Journal of Medical Genetics, Part A
Genetics
Genotype-Phenotype Correlation Analysis of MYO15A Variants in Autosomal Recessive Non-Syndromic Hearing Loss
BMC Medical Genetics
Genetics
Substitutions in the Conserved C2C Domain of Otoferlin Cause DFNB9, a Form of Nonsyndromic Autosomal Recessive Deafness
Neurobiology of Disease
Neurology
Novel Mutations of TMPRSS3 in Four DFNB8/B10 Families Segregating Congenital Autosomal Recessive Deafness
Journal of Medical Genetics
Genetics
Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss
Zahedan Journal of Research in Medical Sciences
A Novel Locus for Autosomal Dominant Nonsyndromic Hearing Loss, DFNA50, Maps to Chromosome 7q32 Between the DFNB17 and DFNB13 Deafness Loci
Journal of Medical Genetics
Genetics
