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T B Friedman

Showing results (71-80 of 86) with videos related to

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The New England Journal of Medicine|November 20, 1998
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafnessR J Morell, H J Kim, L J Hood, et al.
Science (New York, N.Y.)|June 20, 1998
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, et al.
Journal of Medical Genetics|October 22, 2003
Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type IIIS L Ness, T Ben-Yosef, A Bar-Lev, et al.
Journal of Medical Genetics|February 7, 2006
Mutations of human TMHS cause recessively inherited non-syndromic hearing lossM I Shabbir, Z M Ahmed, S Y Khan, et al.
Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.
Science (New York, N.Y.)|June 20, 1998
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgeneF J Probst, R A Fridell, Y Raphael, et al.
Clinical Genetics|September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.
Human Genetics|December 6, 2001
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeN Liburd, M Ghosh, S Riazuddin, 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.
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.
Pageof 9

Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
The New England Journal of Medicine|November 20, 1998
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafnessR J Morell, H J Kim, L J Hood, et al.
Science (New York, N.Y.)|June 20, 1998
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, et al.
Journal of Medical Genetics|October 22, 2003
Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type IIIS L Ness, T Ben-Yosef, A Bar-Lev, et al.
Journal of Medical Genetics|February 7, 2006
Mutations of human TMHS cause recessively inherited non-syndromic hearing lossM I Shabbir, Z M Ahmed, S Y Khan, et al.
Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.
Science (New York, N.Y.)|June 20, 1998
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgeneF J Probst, R A Fridell, Y Raphael, et al.
Clinical Genetics|September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.
Human Genetics|December 6, 2001
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeN Liburd, M Ghosh, S Riazuddin, 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.
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.
Pageof 9