Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J H Smith

Showing results (381-390 of 588) with videos related to

Pageof 59
Sort By:
BMC Nephrology|May 14, 2025
Pregnancy outcomes in C3 glomerulopathy: a retrospective reviewLauren O Fergus, Meryl Waldmann, Monica D Hall, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 30, 2013
C3 glomerulonephritis associated with monoclonal gammopathy: a case seriesLadan Zand, Andrea Kattah, Fernando C Fervenza, et al.
Archives of Disease in Childhood|September 15, 2007
Infant HIV infection despite "universal" antenatal testingS S Struik, G Tudor-Williams, G P Taylor, et al.
Journal of Medical Genetics|June 3, 2004
DFNA5: hearing impairment exon instead of hearing impairment gene?L Van Laer, K Vrijens, S Thys, et al.
American Journal of Human Genetics|May 31, 2016
RNA Interference Prevents Autosomal-Dominant Hearing LossSeiji B Shibata, Paul T Ranum, Hideaki Moteki, et al.
Journal of Medical Genetics|November 14, 2006
Sensorineural deafness and male infertility: a contiguous gene deletion syndromeYuzhou Zhang, Mahdi Malekpour, Navid Al-Madani, et al.
Clinical Genetics|September 9, 2015
Comprehensive genetic testing with ethnic-specific filtering by allele frequency in a Japanese hearing-loss populationH Moteki, H Azaiez, K T Booth, et al.
Advances in Neurobiology|March 12, 2024
Fractal Electronics for Stimulating and Sensing Neural Networks: Enhanced Electrical, Optical, and Cell Interaction PropertiesS Moslehi, C Rowland, J H Smith, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 14, 2010
Dense deposit disease associated with monoclonal gammopathy of undetermined significanceSanjeev Sethi, William R Sukov, Yuzhou Zhang, et al.
Cell|January 16, 2007
Manipulating the mouse genome to engineer precise functional syntenic replacements with human sequenceHelen A C Wallace, Fatima Marques-Kranc, Melville Richardson, et al.
Pageof 59

Showing results (381-390 of 588) with videos related to

Sort By:
Pageof 59
BMC Nephrology|May 14, 2025
Pregnancy outcomes in C3 glomerulopathy: a retrospective reviewLauren O Fergus, Meryl Waldmann, Monica D Hall, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 30, 2013
C3 glomerulonephritis associated with monoclonal gammopathy: a case seriesLadan Zand, Andrea Kattah, Fernando C Fervenza, et al.
Archives of Disease in Childhood|September 15, 2007
Infant HIV infection despite "universal" antenatal testingS S Struik, G Tudor-Williams, G P Taylor, et al.
Journal of Medical Genetics|June 3, 2004
DFNA5: hearing impairment exon instead of hearing impairment gene?L Van Laer, K Vrijens, S Thys, et al.
American Journal of Human Genetics|May 31, 2016
RNA Interference Prevents Autosomal-Dominant Hearing LossSeiji B Shibata, Paul T Ranum, Hideaki Moteki, et al.
Journal of Medical Genetics|November 14, 2006
Sensorineural deafness and male infertility: a contiguous gene deletion syndromeYuzhou Zhang, Mahdi Malekpour, Navid Al-Madani, et al.
Clinical Genetics|September 9, 2015
Comprehensive genetic testing with ethnic-specific filtering by allele frequency in a Japanese hearing-loss populationH Moteki, H Azaiez, K T Booth, et al.
Advances in Neurobiology|March 12, 2024
Fractal Electronics for Stimulating and Sensing Neural Networks: Enhanced Electrical, Optical, and Cell Interaction PropertiesS Moslehi, C Rowland, J H Smith, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 14, 2010
Dense deposit disease associated with monoclonal gammopathy of undetermined significanceSanjeev Sethi, William R Sukov, Yuzhou Zhang, et al.
Cell|January 16, 2007
Manipulating the mouse genome to engineer precise functional syntenic replacements with human sequenceHelen A C Wallace, Fatima Marques-Kranc, Melville Richardson, et al.
Pageof 59