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ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties
|
August 25, 2021
Sequential Bilateral Cochlear Implantation in a Child with Severe External, Middle, and Inner Ear Malformations: Surgical Considerations and Practical Aspects
Dejun Zhang, Yongyi Yuan, Yu Su, et al.
Zhonghua Fu Chan Ke Za Zhi
|
July 26, 2011
[Detection of trisomy 21 by quantitative fluorescent PCR in clinical samples undergoing prenatal diagnosis for hereditary hearing loss]
Yan-ping Lu, Jing Cheng, Bing Han, et al.
Plos One
|
November 6, 2014
KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjects
Jiandong Zhao, Yongyi Yuan, Shasha Huang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
March 2, 2011
Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss
Yi Sun, Jing Cheng, Yanping Lu, et al.
Clinical Genetics
|
July 16, 2022
Evolutionary origin of pathogenic GJB2 alleles in China
Yi Jiang, Shasha Huang, Yi Zhang, et al.
Stem Cell Research
|
March 13, 2021
Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene
Xue Gao, Shi-Wei Qiu, Wei-Qian Wang, et al.
International Journal of Pediatric Otorhinolaryngology
|
August 27, 2011
De novo dominant mutation of GJB2 in two Chinese families with nonsyndromic hearing loss
Shasha Huang, Yongyi Yuan, Jun Liu, et al.
Journal of Translational Medicine
|
December 3, 2010
Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2
Yongyi Yuan, Fei Yu, Guojian Wang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery
|
September 25, 2014
[Assessment of the curative effective of cochlear implantation in childer with GJB2-associated NSSNHL]
Chaochan Cai, Shasha Huang, Xue Gao, et al.
Gene
|
June 23, 2015
Correlation analysis of phenotype and genotype of GJB2 in patients with non-syndromic hearing loss in China
Zhi-Yao Dai, Bao-Chun Sun, Sha-Sha Huang, et al.
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of 22
Search research articles
Search
Showing results (81-90 of 218) with videos related to
Sort By:
Page
of 22
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties
|
August 25, 2021
Sequential Bilateral Cochlear Implantation in a Child with Severe External, Middle, and Inner Ear Malformations: Surgical Considerations and Practical Aspects
Dejun Zhang, Yongyi Yuan, Yu Su, et al.
Zhonghua Fu Chan Ke Za Zhi
|
July 26, 2011
[Detection of trisomy 21 by quantitative fluorescent PCR in clinical samples undergoing prenatal diagnosis for hereditary hearing loss]
Yan-ping Lu, Jing Cheng, Bing Han, et al.
Plos One
|
November 6, 2014
KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjects
Jiandong Zhao, Yongyi Yuan, Shasha Huang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
March 2, 2011
Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss
Yi Sun, Jing Cheng, Yanping Lu, et al.
Clinical Genetics
|
July 16, 2022
Evolutionary origin of pathogenic GJB2 alleles in China
Yi Jiang, Shasha Huang, Yi Zhang, et al.
Stem Cell Research
|
March 13, 2021
Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene
Xue Gao, Shi-Wei Qiu, Wei-Qian Wang, et al.
International Journal of Pediatric Otorhinolaryngology
|
August 27, 2011
De novo dominant mutation of GJB2 in two Chinese families with nonsyndromic hearing loss
Shasha Huang, Yongyi Yuan, Jun Liu, et al.
Journal of Translational Medicine
|
December 3, 2010
Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2
Yongyi Yuan, Fei Yu, Guojian Wang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery
|
September 25, 2014
[Assessment of the curative effective of cochlear implantation in childer with GJB2-associated NSSNHL]
Chaochan Cai, Shasha Huang, Xue Gao, et al.
Gene
|
June 23, 2015
Correlation analysis of phenotype and genotype of GJB2 in patients with non-syndromic hearing loss in China
Zhi-Yao Dai, Bao-Chun Sun, Sha-Sha Huang, et al.
Page
of 22