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Toplam kayıt 25, listelenen: 21-25
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Comprehensive Analysis Via Exome Sequencing Uncovers Genetic Etiology In Autosomal Recessive Non-Syndromic Deafness In A Large Multiethnic Cohort
(2016)Purpose Autosomal recessive non-syndromic deafness (ARNSD) is characterized by a high degree of genetic heterogeneity with reported mutations in 58 different genes. This study was designed to detect deafness causing variants ... -
Variations In Multiple Syndromic Deafness Genes Mimic Non-Syndromic Hearing Loss
(2016)The genetics of both syndromic (SHL) and non-syndromic hearing loss (NSHL) is characterized by a high degree of genetic heterogeneity. We analyzed whole exome sequencing data of 102 unrelated probands with apparently NSHL ... -
Audiological And Radiological Characteristics In Incomplete Partition Malformations
(Aves, 2017)OBJECTIVE: To compare the audiological and radiological findings of patients with incomplete partition malformations (IPs) and analyze the relationship between the audiological and radiological findings. MATERIALS and ... -
Effect of Consonant Duration on Formation of Consonant-Vowel Syllable Evoked Auditory Cortical Potentials
(Aves, 2018)OBJECTIVE: To compare P1-N1-P2-N2 response latencies and amplitudes evoked by voiced and unvoiced consonant-vowel syllables (CVS) /bi/-/pi/ and /di/-/ti/by analyzing how the cortical responses to consonants and vowels ... -
Submucous Cleft Palate: From Diagnosis to Management
(Tubitak Scientific & Technical Research Council Turkey, 2018)Background/aim: The aim of this study was to investigate submucous cleft palate (SMCP) patients in order to document the age of diagnosis, cause of referral, symptoms and palate findings, objective evaluation of nasalance ...