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J H Smith

Showing results (331-340 of 588) with videos related to

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Hearing Research|May 3, 2011
Viral vector tropism for supporting cells in the developing murine cochleaAbraham M Sheffield, Samuel P Gubbels, Michael S Hildebrand, et al.
The Laryngoscope|December 10, 2020
Rigid Video Laryngoscopy for Intubation in Severe Pierre Robin Sequence: A Retrospective ReviewJoseph D Peterson, Michael D Puricelli, Ahmed Alkhateeb, et al.
BMJ Case Reports|June 21, 2011
Sensorineural deafness and male infertility: a contiguous gene deletion syndromeYuzhou Zhang, Mahdi Malekpour, Navid Al-Madani, et al.
American Journal of Human Genetics|April 7, 2009
Human male infertility caused by mutations in the CATSPER1 channel proteinMatthew R Avenarius, Michael S Hildebrand, Yuzhou Zhang, et al.
Auris, Nasus, Larynx|August 9, 2002
High-throughput screening for GJB2 mutations--its clinical application to genetic testing in prelingual deafness screening for GJB2 mutationsAkemi Sugata, Kunihiro Fukushima, Ken-ichi Sugata, et al.
Human Mutation|March 12, 2008
SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BORAmit Kochhar, Dana J Orten, Jessica L Sorensen, et al.
The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
Mutations in LOXHD1 gene cause various types and severities of hearing lossKentaro Mori, Hideaki Moteki, Yumiko Kobayashi, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
A novel splice site mutation in EYA4 causes DFNA10 hearing lossMichael S Hildebrand, David Coman, Tao Yang, et al.
Clinical Journal of the American Society of Nephrology : CJASN|October 25, 2014
Defining the complement biomarker profile of C3 glomerulopathyYuzhou Zhang, Carla M Nester, Bertha Martin, et al.
Journal of the American Society of Nephrology : JASN|December 21, 2013
Clinical findings, pathology, and outcomes of C3GN after kidney transplantationLadan Zand, Elizabeth C Lorenz, Fernando G Cosio, et al.
Pageof 59

Showing results (331-340 of 588) with videos related to

Sort By:
Pageof 59
Hearing Research|May 3, 2011
Viral vector tropism for supporting cells in the developing murine cochleaAbraham M Sheffield, Samuel P Gubbels, Michael S Hildebrand, et al.
The Laryngoscope|December 10, 2020
Rigid Video Laryngoscopy for Intubation in Severe Pierre Robin Sequence: A Retrospective ReviewJoseph D Peterson, Michael D Puricelli, Ahmed Alkhateeb, et al.
BMJ Case Reports|June 21, 2011
Sensorineural deafness and male infertility: a contiguous gene deletion syndromeYuzhou Zhang, Mahdi Malekpour, Navid Al-Madani, et al.
American Journal of Human Genetics|April 7, 2009
Human male infertility caused by mutations in the CATSPER1 channel proteinMatthew R Avenarius, Michael S Hildebrand, Yuzhou Zhang, et al.
Auris, Nasus, Larynx|August 9, 2002
High-throughput screening for GJB2 mutations--its clinical application to genetic testing in prelingual deafness screening for GJB2 mutationsAkemi Sugata, Kunihiro Fukushima, Ken-ichi Sugata, et al.
Human Mutation|March 12, 2008
SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BORAmit Kochhar, Dana J Orten, Jessica L Sorensen, et al.
The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
Mutations in LOXHD1 gene cause various types and severities of hearing lossKentaro Mori, Hideaki Moteki, Yumiko Kobayashi, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
A novel splice site mutation in EYA4 causes DFNA10 hearing lossMichael S Hildebrand, David Coman, Tao Yang, et al.
Clinical Journal of the American Society of Nephrology : CJASN|October 25, 2014
Defining the complement biomarker profile of C3 glomerulopathyYuzhou Zhang, Carla M Nester, Bertha Martin, et al.
Journal of the American Society of Nephrology : JASN|December 21, 2013
Clinical findings, pathology, and outcomes of C3GN after kidney transplantationLadan Zand, Elizabeth C Lorenz, Fernando G Cosio, et al.
Pageof 59