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Showing results (721-730 of 1,165) with videos related to

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Plos Biology|December 3, 2020
Primate phylogenomics uncovers multiple rapid radiations and ancient interspecific introgressionDan Vanderpool, Bui Quang Minh, Robert Lanfear, et al.
Pediatric Diabetes|August 13, 2021
Exome sequencing in children with clinically suspected maturity-onset diabetes of the youngMustafa Tosur, Claudia Soler-Alfonso, Katie M Chan, et al.
Biorxiv : the Preprint Server for Biology|September 16, 2024
Examining intra-host genetic variation of RSV by short read high-throughput sequencingDavid Henke, Felipe-Andrés Piedra, Vasanthi Avadhanula, et al.
Source Code for Biology and Medicine|June 23, 2016
SV-STAT accurately detects structural variation via alignment to reference-based assembliesCaleb F Davis, Deborah I Ritter, David A Wheeler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2016
Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2Samin A Sajan, Shalini N Jhangiani, Donna M Muzny, et al.
Genome Medicine|July 22, 2015
Secondary findings and carrier test frequencies in a large multiethnic sampleTomasz Gambin, Shalini N Jhangiani, Jennifer E Below, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
Nature Genetics|April 28, 2015
Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic diseaseAlexander H Li, Alanna C Morrison, Christie Kovar, et al.
Molecular Vision|January 6, 2012
Exome capture sequencing identifies a novel mutation in BBS4Hui Wang, Xianfeng Chen, Lynn Dudinsky, et al.
American Journal of Medical Genetics. Part A|February 5, 2021
Neurodevelopmental disorder in an Egyptian family with a biallelic ALKBH8 variantAhmed K Saad, Dana Marafi, Tadahiro Mitani, et al.
Pageof 117

Showing results (721-730 of 1,165) with videos related to

Sort By:
Pageof 117
Plos Biology|December 3, 2020
Primate phylogenomics uncovers multiple rapid radiations and ancient interspecific introgressionDan Vanderpool, Bui Quang Minh, Robert Lanfear, et al.
Pediatric Diabetes|August 13, 2021
Exome sequencing in children with clinically suspected maturity-onset diabetes of the youngMustafa Tosur, Claudia Soler-Alfonso, Katie M Chan, et al.
Biorxiv : the Preprint Server for Biology|September 16, 2024
Examining intra-host genetic variation of RSV by short read high-throughput sequencingDavid Henke, Felipe-Andrés Piedra, Vasanthi Avadhanula, et al.
Source Code for Biology and Medicine|June 23, 2016
SV-STAT accurately detects structural variation via alignment to reference-based assembliesCaleb F Davis, Deborah I Ritter, David A Wheeler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2016
Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2Samin A Sajan, Shalini N Jhangiani, Donna M Muzny, et al.
Genome Medicine|July 22, 2015
Secondary findings and carrier test frequencies in a large multiethnic sampleTomasz Gambin, Shalini N Jhangiani, Jennifer E Below, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
Nature Genetics|April 28, 2015
Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic diseaseAlexander H Li, Alanna C Morrison, Christie Kovar, et al.
Molecular Vision|January 6, 2012
Exome capture sequencing identifies a novel mutation in BBS4Hui Wang, Xianfeng Chen, Lynn Dudinsky, et al.
American Journal of Medical Genetics. Part A|February 5, 2021
Neurodevelopmental disorder in an Egyptian family with a biallelic ALKBH8 variantAhmed K Saad, Dana Marafi, Tadahiro Mitani, et al.
Pageof 117