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Carla Nishimura

Showing results (1-10 of 23) with videos related to

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The Laryngoscope|January 28, 2020
Genetic Testing for Congenital Bilateral Hearing Loss in the Context of Targeted Cytomegalovirus ScreeningJoseph Peterson, Carla Nishimura, Richard J H Smith
American Journal of Human Genetics|May 2, 2003
Association of specific language impairment (SLI) to the region of 7q31Erin K O'Brien, Xuyang Zhang, Carla Nishimura, et al.
Journal of Genetics|September 9, 2008
GJB2 mutations in Baluchi populationAnoosh Naghavi, Carla Nishimura, Kimia Kahrizi, et al.
Human Genetics|July 16, 2013
Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genesPatrick D Brophy, Fatemeh Alasti, Benjamin W Darbro, et al.
Human Mutation|December 22, 2017
Exonic mutations and exon skipping: Lessons learned from DFNA5Kevin T Booth, Hela Azaiez, Kimia Kahrizi, et al.
Journal of the American Society of Nephrology : JASN|July 26, 2011
Allelic variants of complement genes associated with dense deposit diseaseMaria Asuncion Abrera-Abeleda, Carla Nishimura, Kathy Frees, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 7, 2012
Causes of alternative pathway dysregulation in dense deposit diseaseYuzhou Zhang, Nicole C Meyer, Kai Wang, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|June 22, 2021
Genetic Causes of Hearing Loss in a Large Cohort of Cochlear Implant RecipientsKristen L Seligman, A Eliot Shearer, Kathy Frees, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Did the GJB2 35delG mutation originate in Iran?Vahideh Norouzi, Hiva Azizi, Zohreh Fattahi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 23, 2008
Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locusMichael S Hildebrand, Dylan Tack, Sarah J McMordie, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
The Laryngoscope|January 28, 2020
Genetic Testing for Congenital Bilateral Hearing Loss in the Context of Targeted Cytomegalovirus ScreeningJoseph Peterson, Carla Nishimura, Richard J H Smith
American Journal of Human Genetics|May 2, 2003
Association of specific language impairment (SLI) to the region of 7q31Erin K O'Brien, Xuyang Zhang, Carla Nishimura, et al.
Journal of Genetics|September 9, 2008
GJB2 mutations in Baluchi populationAnoosh Naghavi, Carla Nishimura, Kimia Kahrizi, et al.
Human Genetics|July 16, 2013
Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genesPatrick D Brophy, Fatemeh Alasti, Benjamin W Darbro, et al.
Human Mutation|December 22, 2017
Exonic mutations and exon skipping: Lessons learned from DFNA5Kevin T Booth, Hela Azaiez, Kimia Kahrizi, et al.
Journal of the American Society of Nephrology : JASN|July 26, 2011
Allelic variants of complement genes associated with dense deposit diseaseMaria Asuncion Abrera-Abeleda, Carla Nishimura, Kathy Frees, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 7, 2012
Causes of alternative pathway dysregulation in dense deposit diseaseYuzhou Zhang, Nicole C Meyer, Kai Wang, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|June 22, 2021
Genetic Causes of Hearing Loss in a Large Cohort of Cochlear Implant RecipientsKristen L Seligman, A Eliot Shearer, Kathy Frees, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Did the GJB2 35delG mutation originate in Iran?Vahideh Norouzi, Hiva Azizi, Zohreh Fattahi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 23, 2008
Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locusMichael S Hildebrand, Dylan Tack, Sarah J McMordie, et al.
Pageof 3