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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 men
Csilla 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 Azoospermia
Liina Nagirnaja, Nina Mørup, John E Nielsen, et al.
The Journal of Pediatrics
|
May 22, 2016
Defining the Phenotype and Assessing Severity in Phosphoglucomutase-1 Deficiency
Sunnie 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 sequencing
Andrew 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 azoospermia
Noor 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 infertility
Kristiina 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 function
Mariam Okhovat, Jake VanCampen, Ana C Lima, et al.
Nature
|
October 9, 2009
Origins and functional impact of copy number variation in the human genome
Donald 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 function
Mariam 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 failure
Antoni Riera-Escamilla, Matthias Vockel, Liina Nagirnaja, et al.
Page
of 38
Search research articles
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Showing results (341-350 of 376) with videos related to
Sort By:
Page
of 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 men
Csilla 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 Azoospermia
Liina Nagirnaja, Nina Mørup, John E Nielsen, et al.
The Journal of Pediatrics
|
May 22, 2016
Defining the Phenotype and Assessing Severity in Phosphoglucomutase-1 Deficiency
Sunnie 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 sequencing
Andrew 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 azoospermia
Noor 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 infertility
Kristiina 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 function
Mariam Okhovat, Jake VanCampen, Ana C Lima, et al.
Nature
|
October 9, 2009
Origins and functional impact of copy number variation in the human genome
Donald 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 function
Mariam 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 failure
Antoni Riera-Escamilla, Matthias Vockel, Liina Nagirnaja, et al.
Page
of 38