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A Muskett

Showing results (11-20 of 18) with videos related to

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The Laryngoscope|November 19, 2016
Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4Jane Rose, Julie A Muskett, Kelly A King, et al.
Journal of Medical Genetics|July 7, 2009
Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypesB Y Choi, A C Madeo, K A King, et al.
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.
JAMA Otolaryngology-- Head & Neck Surgery|September 21, 2013
Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueductParna Chattaraj, Fabian R Reimold, Julie A Muskett, et al.
The Laryngoscope|October 21, 2015
Atypical patterns of segregation of familial enlargement of the vestibular aqueductJulie A Muskett, Parna Chattaraj, John F Heneghan, 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.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2017
<i>NLRP3</i> mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapyHiroshi Nakanishi, Yoshiyuki Kawashima, Kiyoto Kurima, et al.
Journal of Medical Genetics|September 24, 2011
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotesJulie M Schultz, Rashid Bhatti, Anne C Madeo, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
The Laryngoscope|November 19, 2016
Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4Jane Rose, Julie A Muskett, Kelly A King, et al.
Journal of Medical Genetics|July 7, 2009
Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypesB Y Choi, A C Madeo, K A King, et al.
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.
JAMA Otolaryngology-- Head & Neck Surgery|September 21, 2013
Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueductParna Chattaraj, Fabian R Reimold, Julie A Muskett, et al.
The Laryngoscope|October 21, 2015
Atypical patterns of segregation of familial enlargement of the vestibular aqueductJulie A Muskett, Parna Chattaraj, John F Heneghan, 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.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2017
<i>NLRP3</i> mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapyHiroshi Nakanishi, Yoshiyuki Kawashima, Kiyoto Kurima, et al.
Journal of Medical Genetics|September 24, 2011
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotesJulie M Schultz, Rashid Bhatti, Anne C Madeo, et al.
Pageof 2