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G Biesecker

Showing results (411-420 of 475) with videos related to

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Carcinogenesis|October 27, 2025
Symposium report-ethical and social considerations regarding return of secondary findings in atomic bomb survivorsNoriaki Yoshida, Douglas R Stewart, Arikuni Uchimura, et al.
American Journal of Human Genetics|November 15, 2011
Whole-exome-sequencing identifies mutations in histone acetyltransferase gene KAT6B in individuals with the Say-Barber-Biesecker variant of Ohdo syndromeJill Clayton-Smith, James O'Sullivan, Sarah Daly, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2012
Exploring concordance and discordance for return of incidental findings from clinical sequencingRobert C Green, Jonathan S Berg, Gerard T Berry, et al.
Human Mutation|June 10, 2020
An assessment of the role of vinculin loss of function variants in inherited cardiomyopathyMegan H Hawley, Naif Almontashiri, Leslie G Biesecker, et al.
Science (New York, N.Y.)|November 19, 2005
Epidemiology. DNA identifications after the 9/11 World Trade Center attackLeslie G Biesecker, Joan E Bailey-Wilson, Jack Ballantyne, et al.
Journal of Medical Genetics|March 8, 2019
<i>NAA10</i> polyadenylation signal variants cause syndromic microphthalmiaJennifer J Johnston, Kathleen A Williamson, Christopher M Chou, et al.
American Journal of Human Genetics|June 6, 2015
Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutationsJennifer J Johnston, Katie L Lewis, David Ng, et al.
Clinical Genetics|July 9, 2021
A standard of care for individuals with PIK3CA-related disorders: An international expert consensus statementSofia Douzgou, Myfanwy Rawson, Eulalia Baselga, et al.
American Journal of Human Genetics|October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathyHeather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Genetics of growth rate in induced pluripotent stem cellsBrian N Lee, Henry J Taylor, Filippo Cipriani, et al.
Pageof 48

Showing results (411-420 of 475) with videos related to

Sort By:
Pageof 48
Carcinogenesis|October 27, 2025
Symposium report-ethical and social considerations regarding return of secondary findings in atomic bomb survivorsNoriaki Yoshida, Douglas R Stewart, Arikuni Uchimura, et al.
American Journal of Human Genetics|November 15, 2011
Whole-exome-sequencing identifies mutations in histone acetyltransferase gene KAT6B in individuals with the Say-Barber-Biesecker variant of Ohdo syndromeJill Clayton-Smith, James O'Sullivan, Sarah Daly, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2012
Exploring concordance and discordance for return of incidental findings from clinical sequencingRobert C Green, Jonathan S Berg, Gerard T Berry, et al.
Human Mutation|June 10, 2020
An assessment of the role of vinculin loss of function variants in inherited cardiomyopathyMegan H Hawley, Naif Almontashiri, Leslie G Biesecker, et al.
Science (New York, N.Y.)|November 19, 2005
Epidemiology. DNA identifications after the 9/11 World Trade Center attackLeslie G Biesecker, Joan E Bailey-Wilson, Jack Ballantyne, et al.
Journal of Medical Genetics|March 8, 2019
<i>NAA10</i> polyadenylation signal variants cause syndromic microphthalmiaJennifer J Johnston, Kathleen A Williamson, Christopher M Chou, et al.
American Journal of Human Genetics|June 6, 2015
Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutationsJennifer J Johnston, Katie L Lewis, David Ng, et al.
Clinical Genetics|July 9, 2021
A standard of care for individuals with PIK3CA-related disorders: An international expert consensus statementSofia Douzgou, Myfanwy Rawson, Eulalia Baselga, et al.
American Journal of Human Genetics|October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathyHeather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Genetics of growth rate in induced pluripotent stem cellsBrian N Lee, Henry J Taylor, Filippo Cipriani, et al.
Pageof 48