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Pu Dai

Showing results (211-220 of 218) with videos related to

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Physiological Genomics|June 11, 2009
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing lossPu Dai, Andrew K Stewart, Fouad Chebib, et al.
Frontiers in Cardiovascular Medicine|November 21, 2022
Analysis of influencing factors for prognosis of patients with ventricular septal perforation: A single-center retrospective studyMing-Xuan Duan, Xi Zhao, Shao-Lin Li, et al.
Journal of Medical Genetics|February 18, 2018
Mutation of <i>IFNLR1</i>, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing lossXue Gao, Yong-Yi Yuan, Qiong-Fen Lin, et al.
American Journal of Human Genetics|December 22, 2009
Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2Xuezhong Liu, Dongyi Han, Jianzhong Li, et al.
Journal of Translational Medicine|April 16, 2009
GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairmentPu Dai, Fei Yu, Bing Han, et al.
JAMA Otolaryngology-- Head & Neck Surgery|August 29, 2020
Unilateral Cochlear Implants for Severe, Profound, or Moderate Sloping to Profound Bilateral Sensorineural Hearing Loss: A Systematic Review and Consensus StatementsCraig A Buchman, René H Gifford, David S Haynes, et al.
American Journal of Human Genetics|October 1, 2019
Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, ChinaPu Dai, Li-Hui Huang, Guo-Jian Wang, et al.
Human Genetics|May 1, 2024
The natural history and genotype-phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysisBrett M Colbert, Cris Lanting, Molly Smeal, et al.
Pageof 22

Showing results (211-220 of 218) with videos related to

Sort By:
Pageof 22
You have reached the last page of results.This site can display upto 218 results.
Physiological Genomics|June 11, 2009
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing lossPu Dai, Andrew K Stewart, Fouad Chebib, et al.
Frontiers in Cardiovascular Medicine|November 21, 2022
Analysis of influencing factors for prognosis of patients with ventricular septal perforation: A single-center retrospective studyMing-Xuan Duan, Xi Zhao, Shao-Lin Li, et al.
Journal of Medical Genetics|February 18, 2018
Mutation of <i>IFNLR1</i>, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing lossXue Gao, Yong-Yi Yuan, Qiong-Fen Lin, et al.
American Journal of Human Genetics|December 22, 2009
Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2Xuezhong Liu, Dongyi Han, Jianzhong Li, et al.
Journal of Translational Medicine|April 16, 2009
GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairmentPu Dai, Fei Yu, Bing Han, et al.
JAMA Otolaryngology-- Head & Neck Surgery|August 29, 2020
Unilateral Cochlear Implants for Severe, Profound, or Moderate Sloping to Profound Bilateral Sensorineural Hearing Loss: A Systematic Review and Consensus StatementsCraig A Buchman, René H Gifford, David S Haynes, et al.
American Journal of Human Genetics|October 1, 2019
Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, ChinaPu Dai, Li-Hui Huang, Guo-Jian Wang, et al.
Human Genetics|May 1, 2024
The natural history and genotype-phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysisBrett M Colbert, Cris Lanting, Molly Smeal, et al.
Pageof 22