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Deliang Huang

Showing results (61-70 of 68) with videos related to

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Allergy|April 3, 2020
COVID-19 in a designated infectious diseases hospital outside Hubei Province, ChinaQingxian Cai, Deliang Huang, Pengcheng Ou, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2007
The prevalence of the 235delC GJB2 mutation in a Chinese deaf populationPu Dai, Fei Yu, Bing Han, et al.
Journal of Hepatology|April 17, 2020
COVID-19: Abnormal liver function testsQingxian Cai, Deliang Huang, Hong Yu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2008
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing lossPu Dai, Qi Li, Deliang Huang, et al.
Biochemical and Biophysical Research Communications|December 27, 2005
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafnessPu Dai, Xin Liu, Dongyi Han, et al.
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.
Engineering (Beijing, China)|April 30, 2020
Experimental Treatment with Favipiravir for COVID-19: An Open-Label Control StudyQingxian Cai, Minghui Yang, Dongjing Liu, 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.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Allergy|April 3, 2020
COVID-19 in a designated infectious diseases hospital outside Hubei Province, ChinaQingxian Cai, Deliang Huang, Pengcheng Ou, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2007
The prevalence of the 235delC GJB2 mutation in a Chinese deaf populationPu Dai, Fei Yu, Bing Han, et al.
Journal of Hepatology|April 17, 2020
COVID-19: Abnormal liver function testsQingxian Cai, Deliang Huang, Hong Yu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2008
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing lossPu Dai, Qi Li, Deliang Huang, et al.
Biochemical and Biophysical Research Communications|December 27, 2005
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafnessPu Dai, Xin Liu, Dongyi Han, et al.
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.
Engineering (Beijing, China)|April 30, 2020
Experimental Treatment with Favipiravir for COVID-19: An Open-Label Control StudyQingxian Cai, Minghui Yang, Dongjing Liu, 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.
Pageof 7