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J Morell

Showing results (81-90 of 118) with videos related to

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Journal of Medical Genetics|August 7, 2017
A common <i>SLC26A4</i>-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueductParna Chattaraj, Tina Munjal, Keiji Honda, et al.
Clinical Genetics|August 31, 2016
Genetic causes of moderate to severe hearing loss point to modifiersSadaf Naz, Ayesha Imtiaz, Ghulam Mujtaba, et al.
American Journal of Human Genetics|July 30, 2002
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locusSadaf Naz, Chantal M Giguere, David C Kohrman, et al.
American Journal of Human Genetics|April 11, 2003
Mutations of MYO6 are associated with recessive deafness, DFNB37Zubair M Ahmed, Robert J Morell, Saima Riazuddin, et al.
The Journal of Biological Chemistry|September 2, 2020
G protein-coupled receptor <i>Gpr115</i> (<i>Adgrf4</i>) is required for enamel mineralization mediated by ameloblastsYuta Chiba, Keigo Yoshizaki, Kan Saito, 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.
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.
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.
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.
Anales De Pediatria (Barcelona, Spain : 2003)|December 1, 2009
[Allergic sensitization profile in 0-5 year old children with wheezing and/or atopic dermatitis]I Carvajal Urueña, C Díaz Vázquez, A Cano Garcinuño, et al.
Pageof 12

Showing results (81-90 of 118) with videos related to

Sort By:
Pageof 12
Journal of Medical Genetics|August 7, 2017
A common <i>SLC26A4</i>-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueductParna Chattaraj, Tina Munjal, Keiji Honda, et al.
Clinical Genetics|August 31, 2016
Genetic causes of moderate to severe hearing loss point to modifiersSadaf Naz, Ayesha Imtiaz, Ghulam Mujtaba, et al.
American Journal of Human Genetics|July 30, 2002
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locusSadaf Naz, Chantal M Giguere, David C Kohrman, et al.
American Journal of Human Genetics|April 11, 2003
Mutations of MYO6 are associated with recessive deafness, DFNB37Zubair M Ahmed, Robert J Morell, Saima Riazuddin, et al.
The Journal of Biological Chemistry|September 2, 2020
G protein-coupled receptor <i>Gpr115</i> (<i>Adgrf4</i>) is required for enamel mineralization mediated by ameloblastsYuta Chiba, Keigo Yoshizaki, Kan Saito, 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.
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.
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.
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.
Anales De Pediatria (Barcelona, Spain : 2003)|December 1, 2009
[Allergic sensitization profile in 0-5 year old children with wheezing and/or atopic dermatitis]I Carvajal Urueña, C Díaz Vázquez, A Cano Garcinuño, et al.
Pageof 12