Muzeyyen Baylan-Yildirim
Dicle, Turkey
Last Updated: 09/26/2026
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Found 10 publications
Identifying DNA Variants in a Turkish Cohort with Inner Ear Anomalies.
Journal: Ear, nose, & throat journal
Published: October 26, 2024
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss.
Journal: Journal of human genetics
Published: October 10, 2022
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 21, 2022
A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss.
Journal: Human genetics
Published: April 16, 2019
Three cases of Chronic Suppurative Otitis Media (CSOM) caused by Kerstersia gyiorum and a review of the literature.
Journal: Le infezioni in medicina
Published: December 18, 2018
Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss.
Journal: Scientific reports
Published: April 27, 2016
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 27, 2015
Evidence for genotype-phenotype correlation for OTOF mutations.
Journal: International journal of pediatric otorhinolaryngology
Published: November 12, 2013
Ectodermal dysplasia: otolaryngologic evaluation of 23 cases.
Journal: Ear, nose, & throat journal
Published: February 24, 2012
Is preeclampsia a new risk factor for cochlear damage and hearing loss?
Journal: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology
Published: July 27, 2010
Showing 1-10 of 10
Last Updated: 09/26/2026