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Denise Yan

Showing results (11-20 of 103) with videos related to

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International Journal of Pediatric Otorhinolaryngology|December 31, 2017
A novel splicing mutation in SMPX is linked to nonsyndromic progressive hearing lossZhijie Niu, Denise Yan, Sara Bressler, et al.
The Laryngoscope|October 9, 2019
Progressive Dominant Hearing Loss (Autosomal Dominant Deafness-41) and P2RX2 Gene Mutations: A Phenotype-Genotype StudyXue Zhong Liu, Denise Yan, Rahul Mittal, et al.
Frontiers in Audiology and Otology|April 9, 2024
Responsiveness of the electrically stimulated cochlear nerve in patients with a missense variant in <i>ACTG1</i>: Preliminary ResultsYi Yuan, Denise Yan, Jeffrey Skidmore, et al.
American Journal of Medical Genetics. Part A|January 30, 2007
Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing lossDenise Yan, Xiao Mei Ouyang, Simon I Angeli, et al.
The Laryngoscope|February 3, 2011
Clinical comparison of hearing-impaired patients with DFNB1 against heterozygote carriers of connexin 26 mutationsMichael Lipan, Xiaomei Ouyang, Denise Yan, et al.
Frontiers in Genetics|December 19, 2019
Recent Perspectives on Gene-Microbe Interactions Determining Predisposition to Otitis MediaRahul Mittal, Sebastian V Sanchez-Luege, Shannon M Wagner, et al.
Gene|November 4, 2018
Role of microRNAs in inner ear development and hearing lossRahul Mittal, George Liu, Sai P Polineni, et al.
Disease Markers|June 20, 2015
Association of PRPS1 Mutations with Disease PhenotypesRahul Mittal, Kunal Patel, Jeenu Mittal, et al.
International Journal of Audiology|July 3, 2019
Genetic screening as an adjunct to universal newborn hearing screening: literature review and implications for non-congenital pre-lingual hearing lossChristine D'Aguillo, Sara Bressler, Denise Yan, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|July 13, 2012
Etiologic diagnosis of nonsyndromic genetic hearing loss in adult vs pediatric populationsPeter J King, Xiaomei Ouyang, Lilin Du, et al.
Pageof 11

Showing results (11-20 of 103) with videos related to

Sort By:
Pageof 11
International Journal of Pediatric Otorhinolaryngology|December 31, 2017
A novel splicing mutation in SMPX is linked to nonsyndromic progressive hearing lossZhijie Niu, Denise Yan, Sara Bressler, et al.
The Laryngoscope|October 9, 2019
Progressive Dominant Hearing Loss (Autosomal Dominant Deafness-41) and P2RX2 Gene Mutations: A Phenotype-Genotype StudyXue Zhong Liu, Denise Yan, Rahul Mittal, et al.
Frontiers in Audiology and Otology|April 9, 2024
Responsiveness of the electrically stimulated cochlear nerve in patients with a missense variant in <i>ACTG1</i>: Preliminary ResultsYi Yuan, Denise Yan, Jeffrey Skidmore, et al.
American Journal of Medical Genetics. Part A|January 30, 2007
Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing lossDenise Yan, Xiao Mei Ouyang, Simon I Angeli, et al.
The Laryngoscope|February 3, 2011
Clinical comparison of hearing-impaired patients with DFNB1 against heterozygote carriers of connexin 26 mutationsMichael Lipan, Xiaomei Ouyang, Denise Yan, et al.
Frontiers in Genetics|December 19, 2019
Recent Perspectives on Gene-Microbe Interactions Determining Predisposition to Otitis MediaRahul Mittal, Sebastian V Sanchez-Luege, Shannon M Wagner, et al.
Gene|November 4, 2018
Role of microRNAs in inner ear development and hearing lossRahul Mittal, George Liu, Sai P Polineni, et al.
Disease Markers|June 20, 2015
Association of PRPS1 Mutations with Disease PhenotypesRahul Mittal, Kunal Patel, Jeenu Mittal, et al.
International Journal of Audiology|July 3, 2019
Genetic screening as an adjunct to universal newborn hearing screening: literature review and implications for non-congenital pre-lingual hearing lossChristine D'Aguillo, Sara Bressler, Denise Yan, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|July 13, 2012
Etiologic diagnosis of nonsyndromic genetic hearing loss in adult vs pediatric populationsPeter J King, Xiaomei Ouyang, Lilin Du, et al.
Pageof 11