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Showing results (61-70 of 66) with videos related to

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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.
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.
Poultry Science|December 30, 2022
Effects of selenium supplementation on the growth performance, slaughter characteristics, and blood biochemistry of naked neck chickenM T Khan, A S Niazi, M Arslan, et al.
Journal of Medical Genetics|June 27, 2001
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafnessT Ben-Yosef, M Wattenhofer, S Riazuddin, et al.
Journal of Medical Genetics|April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessH-J Park, S Shaukat, X-Z Liu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 24, 2024
Distinctive sleep complaints and polysomnographic findings in antibody subgroups of autoimmune limbic encephalitisCem İsmail Küçükali, Vuslat Yılmaz, Derya Karadeniz, et al.
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Showing results (61-70 of 66) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 66 results.
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.
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.
Poultry Science|December 30, 2022
Effects of selenium supplementation on the growth performance, slaughter characteristics, and blood biochemistry of naked neck chickenM T Khan, A S Niazi, M Arslan, et al.
Journal of Medical Genetics|June 27, 2001
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafnessT Ben-Yosef, M Wattenhofer, S Riazuddin, et al.
Journal of Medical Genetics|April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessH-J Park, S Shaukat, X-Z Liu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 24, 2024
Distinctive sleep complaints and polysomnographic findings in antibody subgroups of autoimmune limbic encephalitisCem İsmail Küçükali, Vuslat Yılmaz, Derya Karadeniz, et al.
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