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Showing results (341-350 of 376) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic menCsilla Krausz, Antoni Riera-Escamilla, Daniel Moreno-Mendoza, et al.
The New England Journal of Medicine|August 4, 2021
Variant <i>PNLDC1</i>, Defective piRNA Processing, and AzoospermiaLiina Nagirnaja, Nina Mørup, John E Nielsen, et al.
The Journal of Pediatrics|May 22, 2016
Defining the Phenotype and Assessing Severity in Phosphoglucomutase-1 DeficiencySunnie Yan-Wai Wong, Lesa J Beamer, Therese Gadomski, et al.
Plos Genetics|July 11, 2014
Clonal architecture of secondary acute myeloid leukemia defined by single-cell sequencingAndrew E O Hughes, Vincent Magrini, Ryan Demeter, et al.
Journal of Assisted Reproduction and Genetics|August 15, 2025
Identification of missense DMC1 variants in males with non-obstructive azoospermiaNoor Ullah, Christopher Pombar, Rachel Hvasta-Gloria, et al.
American Journal of Human Genetics|April 13, 2024
Toward clinical exomes in diagnostics and management of male infertilityKristiina Lillepea, Anna-Grete Juchnewitsch, Laura Kasak, et al.
Biorxiv : the Preprint Server for Biology|March 22, 2023
TAD Evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and functionMariam Okhovat, Jake VanCampen, Ana C Lima, et al.
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Nature Communications|December 7, 2023
TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and functionMariam Okhovat, Jake VanCampen, Kimberly A Nevonen, et al.
American Journal of Human Genetics|July 9, 2022
Large-scale analyses of the X chromosome in 2,354 infertile men discover recurrently affected genes associated with spermatogenic failureAntoni Riera-Escamilla, Matthias Vockel, Liina Nagirnaja, et al.
Pageof 38

Showing results (341-350 of 376) with videos related to

Sort By:
Pageof 38
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic menCsilla Krausz, Antoni Riera-Escamilla, Daniel Moreno-Mendoza, et al.
The New England Journal of Medicine|August 4, 2021
Variant <i>PNLDC1</i>, Defective piRNA Processing, and AzoospermiaLiina Nagirnaja, Nina Mørup, John E Nielsen, et al.
The Journal of Pediatrics|May 22, 2016
Defining the Phenotype and Assessing Severity in Phosphoglucomutase-1 DeficiencySunnie Yan-Wai Wong, Lesa J Beamer, Therese Gadomski, et al.
Plos Genetics|July 11, 2014
Clonal architecture of secondary acute myeloid leukemia defined by single-cell sequencingAndrew E O Hughes, Vincent Magrini, Ryan Demeter, et al.
Journal of Assisted Reproduction and Genetics|August 15, 2025
Identification of missense DMC1 variants in males with non-obstructive azoospermiaNoor Ullah, Christopher Pombar, Rachel Hvasta-Gloria, et al.
American Journal of Human Genetics|April 13, 2024
Toward clinical exomes in diagnostics and management of male infertilityKristiina Lillepea, Anna-Grete Juchnewitsch, Laura Kasak, et al.
Biorxiv : the Preprint Server for Biology|March 22, 2023
TAD Evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and functionMariam Okhovat, Jake VanCampen, Ana C Lima, et al.
Nature|October 9, 2009
Origins and functional impact of copy number variation in the human genomeDonald F Conrad, Dalila Pinto, Richard Redon, et al.
Nature Communications|December 7, 2023
TAD evolutionary and functional characterization reveals diversity in mammalian TAD boundary properties and functionMariam Okhovat, Jake VanCampen, Kimberly A Nevonen, et al.
American Journal of Human Genetics|July 9, 2022
Large-scale analyses of the X chromosome in 2,354 infertile men discover recurrently affected genes associated with spermatogenic failureAntoni Riera-Escamilla, Matthias Vockel, Liina Nagirnaja, et al.
Pageof 38