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Showing results (891-900 of 968) with videos related to

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Cell|February 13, 2001
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29E R Wilcox, Q L Burton, S Naz, et al.
Psychiatry Research|July 8, 2025
Prenatal obsessive beliefs predict postpartum obsessive-compulsive symptoms: a prospective studyJonathan S Abramowitz, Samantha N Hellberg, Janice Krasnow, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 8, 2014
Communication gaps associated with donor-derived infectionsR Miller, S Covington, S Taranto, et al.
Science (New York, N.Y.)|April 16, 1998
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humansO Vahava, R Morell, E D Lynch, et al.
European Journal of Human Genetics : EJHG|February 18, 2016
Heritability of non-speech auditory processing skillsCarmen C Brewer, Christopher K Zalewski, Kelly A King, et al.
Human Mutation|July 5, 2016
Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human DeafnessAtteeq U Rehman, Jonathan E Bird, Rabia Faridi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 30, 2006
The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15Zubair M Ahmed, Richard Goodyear, Saima Riazuddin, et al.
Human Mutation|June 5, 2007
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearingNevra Nal, Zubair M Ahmed, Engin Erkal, et al.
Human Mutation|November 22, 2018
Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward SyndromeRabia Faridi, Risa Tona, Alessandra Brofferio, et al.
Investigative Ophthalmology & Visual Science|November 27, 2014
Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinographyWadih M Zein, Benedetto Falsini, Ekaterina T Tsilou, et al.
Pageof 97

Showing results (891-900 of 968) with videos related to

Sort By:
Pageof 97
Cell|February 13, 2001
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29E R Wilcox, Q L Burton, S Naz, et al.
Psychiatry Research|July 8, 2025
Prenatal obsessive beliefs predict postpartum obsessive-compulsive symptoms: a prospective studyJonathan S Abramowitz, Samantha N Hellberg, Janice Krasnow, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 8, 2014
Communication gaps associated with donor-derived infectionsR Miller, S Covington, S Taranto, et al.
Science (New York, N.Y.)|April 16, 1998
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humansO Vahava, R Morell, E D Lynch, et al.
European Journal of Human Genetics : EJHG|February 18, 2016
Heritability of non-speech auditory processing skillsCarmen C Brewer, Christopher K Zalewski, Kelly A King, et al.
Human Mutation|July 5, 2016
Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human DeafnessAtteeq U Rehman, Jonathan E Bird, Rabia Faridi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 30, 2006
The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15Zubair M Ahmed, Richard Goodyear, Saima Riazuddin, et al.
Human Mutation|June 5, 2007
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearingNevra Nal, Zubair M Ahmed, Engin Erkal, et al.
Human Mutation|November 22, 2018
Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward SyndromeRabia Faridi, Risa Tona, Alessandra Brofferio, et al.
Investigative Ophthalmology & Visual Science|November 27, 2014
Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinographyWadih M Zein, Benedetto Falsini, Ekaterina T Tsilou, et al.
Pageof 97