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Joseph Foster

Showing results (11-20 of 32) with videos related to

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Clinical Case Reports|April 12, 2017
Dominant deafness-onychodystrophy syndrome caused by an <i>ATP6V1B2</i> mutationIbis Menendez, Claudia Carranza, Mariana Herrera, et al.
Arthritis and Rheumatism|May 14, 2013
DNASE1L3 mutations in hypocomplementemic urticarial vasculitis syndromeZ Birsin Ozçakar, Joseph Foster, Oscar Diaz-Horta, et al.
Human Genetics|December 17, 2013
De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsisWilla Thorson, Oscar Diaz-Horta, Joseph Foster, et al.
Hearing Research|February 7, 2016
A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genesDemet Tekin, Denise Yan, Guney Bademci, et al.
Journal of Pediatric Genetics|May 13, 2017
Novel Causative Variants in <i>DYRK1A, KARS</i>, and <i>KAT6A</i> Associated with Intellectual Disability and Additional Phenotypic FeaturesClark R Murray, Samantha N Abel, Matthew B McClure, et al.
Hearing, Balance and Communication|February 26, 2019
Genetic screening revealed usher syndrome in a paediatric Chinese patientChunyan Qu, Fenghe Liang, Qin Long, et al.
Genetic Testing and Molecular Biomarkers|July 26, 2014
Identification of copy number variants through whole-exome sequencing in autosomal recessive nonsyndromic hearing lossGuney Bademci, Oscar Diaz-Horta, Shengru Guo, et al.
Plant Disease|December 9, 2023
First report of three bunya-like viruses, apple luteovirus 1, and apple hammerhead viroid in apples from Hakkari, TürkiyeNevin Akdura, Joshua Mendoza, Samantha Hasselhoff, et al.
Archives of Virology|July 22, 2021
Identification and characterization of a novel virus associated with an eriophyid mite in extracts of fruit trees leavesLarissa Carvalho Costa, Kristian Stevens, Xiaojun Hu, et al.
Archives of Virology|November 10, 2021
Genomic characterization of silvergrass cryptic virus 1, a novel partitivirus infecting Miscanthus sinensisLarissa C Costa, Xiaojun Hu, Martha Malapi-Wight, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Clinical Case Reports|April 12, 2017
Dominant deafness-onychodystrophy syndrome caused by an <i>ATP6V1B2</i> mutationIbis Menendez, Claudia Carranza, Mariana Herrera, et al.
Arthritis and Rheumatism|May 14, 2013
DNASE1L3 mutations in hypocomplementemic urticarial vasculitis syndromeZ Birsin Ozçakar, Joseph Foster, Oscar Diaz-Horta, et al.
Human Genetics|December 17, 2013
De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsisWilla Thorson, Oscar Diaz-Horta, Joseph Foster, et al.
Hearing Research|February 7, 2016
A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genesDemet Tekin, Denise Yan, Guney Bademci, et al.
Journal of Pediatric Genetics|May 13, 2017
Novel Causative Variants in <i>DYRK1A, KARS</i>, and <i>KAT6A</i> Associated with Intellectual Disability and Additional Phenotypic FeaturesClark R Murray, Samantha N Abel, Matthew B McClure, et al.
Hearing, Balance and Communication|February 26, 2019
Genetic screening revealed usher syndrome in a paediatric Chinese patientChunyan Qu, Fenghe Liang, Qin Long, et al.
Genetic Testing and Molecular Biomarkers|July 26, 2014
Identification of copy number variants through whole-exome sequencing in autosomal recessive nonsyndromic hearing lossGuney Bademci, Oscar Diaz-Horta, Shengru Guo, et al.
Plant Disease|December 9, 2023
First report of three bunya-like viruses, apple luteovirus 1, and apple hammerhead viroid in apples from Hakkari, TürkiyeNevin Akdura, Joshua Mendoza, Samantha Hasselhoff, et al.
Archives of Virology|July 22, 2021
Identification and characterization of a novel virus associated with an eriophyid mite in extracts of fruit trees leavesLarissa Carvalho Costa, Kristian Stevens, Xiaojun Hu, et al.
Archives of Virology|November 10, 2021
Genomic characterization of silvergrass cryptic virus 1, a novel partitivirus infecting Miscanthus sinensisLarissa C Costa, Xiaojun Hu, Martha Malapi-Wight, et al.
Pageof 4