Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Seung Ha Oh

Showing results (211-220 of 235) with videos related to

Pageof 24
Sort By:
Scientific Reports|July 21, 2023
Phenotypic and molecular basis of SIX1 variants linked to non-syndromic deafness and atypical branchio-otic syndrome in South KoreaSomin Lee, Yejin Yun, Ju Hyuen Cha, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2015
Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric populationNayoung K D Kim, Ah Reum Kim, Kyung Tae Park, et al.
Molecules and Cells|August 6, 2015
Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome SequencingMun Young Chang, Ah Reum Kim, Nayoung K D Kim, et al.
Scientific Reports|November 20, 2023
Allelic hierarchy for USH2A influences auditory and visual phenotypes in South Korean patientsDong Woo Nam, Yong Keun Song, Jeong Hun Kim, et al.
Molecular Imaging and Biology|April 22, 2008
Assessment of cerebral glucose metabolism in cat deafness model: strategies for improving the voxel-based statistical analysis for animal PET studiesJin Su Kim, Jae Sung Lee, Min-Hyun Park, et al.
Diagnostics (Basel, Switzerland)|September 9, 2020
Flexible Real-Time Polymerase Chain Reaction-Based Platforms for Detecting Deafness Mutations in Koreans: A Proposed Guideline for the Etiologic Diagnosis of Auditory Neuropathy Spectrum DisorderSang-Yeon Lee, Doo-Yi Oh, Jin Hee Han, et al.
Ear and Hearing|April 30, 2021
Natural Course of Residual Hearing with Reference to GJB2 and SLC26A4 Genotypes: Clinical Implications for Hearing RehabilitationSang-Yeon Lee, Seung Cheol Han, Jin Hee Han, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 15, 2014
A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitationJuyong Chung, Sang Min Park, Sun O Chang, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 11, 2014
De novo large genomic deletions involving POU3F4 in incomplete partition type III inner ear anomaly in East Asian populations and implications for genetic counselingJin Woong Choi, ByungJoo Min, AhReum Kim, et al.
Human Mutation|August 26, 2020
Novel genotype-phenotype correlation of functionally characterized LMX1A variants linked to sensorineural hearing lossSang-Yeon Lee, Jin Hee Han, Marge Carandang, et al.
Pageof 24

Showing results (211-220 of 235) with videos related to

Sort By:
Pageof 24
Scientific Reports|July 21, 2023
Phenotypic and molecular basis of SIX1 variants linked to non-syndromic deafness and atypical branchio-otic syndrome in South KoreaSomin Lee, Yejin Yun, Ju Hyuen Cha, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2015
Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric populationNayoung K D Kim, Ah Reum Kim, Kyung Tae Park, et al.
Molecules and Cells|August 6, 2015
Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome SequencingMun Young Chang, Ah Reum Kim, Nayoung K D Kim, et al.
Scientific Reports|November 20, 2023
Allelic hierarchy for USH2A influences auditory and visual phenotypes in South Korean patientsDong Woo Nam, Yong Keun Song, Jeong Hun Kim, et al.
Molecular Imaging and Biology|April 22, 2008
Assessment of cerebral glucose metabolism in cat deafness model: strategies for improving the voxel-based statistical analysis for animal PET studiesJin Su Kim, Jae Sung Lee, Min-Hyun Park, et al.
Diagnostics (Basel, Switzerland)|September 9, 2020
Flexible Real-Time Polymerase Chain Reaction-Based Platforms for Detecting Deafness Mutations in Koreans: A Proposed Guideline for the Etiologic Diagnosis of Auditory Neuropathy Spectrum DisorderSang-Yeon Lee, Doo-Yi Oh, Jin Hee Han, et al.
Ear and Hearing|April 30, 2021
Natural Course of Residual Hearing with Reference to GJB2 and SLC26A4 Genotypes: Clinical Implications for Hearing RehabilitationSang-Yeon Lee, Seung Cheol Han, Jin Hee Han, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 15, 2014
A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitationJuyong Chung, Sang Min Park, Sun O Chang, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 11, 2014
De novo large genomic deletions involving POU3F4 in incomplete partition type III inner ear anomaly in East Asian populations and implications for genetic counselingJin Woong Choi, ByungJoo Min, AhReum Kim, et al.
Human Mutation|August 26, 2020
Novel genotype-phenotype correlation of functionally characterized LMX1A variants linked to sensorineural hearing lossSang-Yeon Lee, Jin Hee Han, Marge Carandang, et al.
Pageof 24