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Katherine O Welch

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

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American Journal of Medical Genetics. Part A|April 14, 2007
Compound heterozygosity for dominant and recessive GJB2 mutations: effect on phenotype and review of the literatureKatherine O Welch, Ruth S Marin, Arti Pandya, et al.
American Journal of Human Genetics|July 29, 2008
A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apartKathleen S Arnos, Katherine O Welch, Mustafa Tekin, et al.
Annals of Human Genetics|November 26, 2009
Fitness among individuals with early childhood deafness: Studies in alumni families from Gallaudet UniversitySusan H Blanton, Walter E Nance, Virginia W Norris, et al.
Current Issues in Molecular Biology|March 28, 2026
E-Cadherin Is an Accurate Target for Fluorescence-Guided Imaging of Lymph NodesKelly A McGovern, Katherine O Welch, Jake Mlakar, et al.
Molecular Imaging and Biology|October 14, 2025
Epithelial Cell Adhesion Molecule Is an Accurate Target for Fluorescence Guided Imaging of Lymph NodesKelly Anne McGovern, Katherine O Welch, Ryan Krouse, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probandsArti Pandya, Kathleen S Arnos, Xia J Xia, et al.
American Journal of Medical Genetics. Part A|April 6, 2011
Vestibular dysfunction in DFNB1 deafnessKelley M Dodson, Susan H Blanton, Katherine O Welch, et al.
Human Mutation|January 29, 2008
Branchio-oto-renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BORDana J Orten, Stephanie M Fischer, Jessica L Sorensen, et al.
Human Molecular Genetics|April 30, 2003
Prestin, a cochlear motor protein, is defective in non-syndromic hearing lossXue Zhong Liu, Xiao Mei Ouyang, Xia Juan Xia, et al.
American Journal of Medical Genetics. Part A|May 4, 2011
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairmentNanna D Rendtorff, Marianne Lodahl, Houda Boulahbel, et al.
Pageof 1

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

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|April 14, 2007
Compound heterozygosity for dominant and recessive GJB2 mutations: effect on phenotype and review of the literatureKatherine O Welch, Ruth S Marin, Arti Pandya, et al.
American Journal of Human Genetics|July 29, 2008
A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apartKathleen S Arnos, Katherine O Welch, Mustafa Tekin, et al.
Annals of Human Genetics|November 26, 2009
Fitness among individuals with early childhood deafness: Studies in alumni families from Gallaudet UniversitySusan H Blanton, Walter E Nance, Virginia W Norris, et al.
Current Issues in Molecular Biology|March 28, 2026
E-Cadherin Is an Accurate Target for Fluorescence-Guided Imaging of Lymph NodesKelly A McGovern, Katherine O Welch, Jake Mlakar, et al.
Molecular Imaging and Biology|October 14, 2025
Epithelial Cell Adhesion Molecule Is an Accurate Target for Fluorescence Guided Imaging of Lymph NodesKelly Anne McGovern, Katherine O Welch, Ryan Krouse, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probandsArti Pandya, Kathleen S Arnos, Xia J Xia, et al.
American Journal of Medical Genetics. Part A|April 6, 2011
Vestibular dysfunction in DFNB1 deafnessKelley M Dodson, Susan H Blanton, Katherine O Welch, et al.
Human Mutation|January 29, 2008
Branchio-oto-renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BORDana J Orten, Stephanie M Fischer, Jessica L Sorensen, et al.
Human Molecular Genetics|April 30, 2003
Prestin, a cochlear motor protein, is defective in non-syndromic hearing lossXue Zhong Liu, Xiao Mei Ouyang, Xia Juan Xia, et al.
American Journal of Medical Genetics. Part A|May 4, 2011
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairmentNanna D Rendtorff, Marianne Lodahl, Houda Boulahbel, et al.
Pageof 1