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HGG Advances
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January 20, 2022
From karyotypes to precision genomics in 9p deletion and duplication syndromes
Eleanor I Sams, Jeffrey K Ng, Victoria Tate, et al.
Human Molecular Genetics
|
September 15, 2023
A common single nucleotide variant in the cytokine receptor-like factor-3 (CRLF3) gene causes neuronal deficits in human and mouse cells
Anna F Wilson, Rasha Barakat, Rui Mu, et al.
Genome Research
|
July 24, 2021
Differences in the number of de novo mutations between individuals are due to small family-specific effects and stochasticity
Jakob M Goldmann, Juliet E Hampstead, Wendy S W Wong, et al.
Oncogene
|
January 27, 2010
Integrative molecular profiling of triple negative breast cancers identifies amplicon drivers and potential therapeutic targets
N Turner, M B Lambros, H M Horlings, et al.
Notfall & Rettungsmedizin
|
June 16, 2020
[Education]
C Lott, F Carmona, P Van de Voorde, et al.
The New England Journal of Medicine
|
April 11, 2019
Molecular Genetic Anatomy and Risk Profile of Hirschsprung's Disease
Joseph M Tilghman, Albee Y Ling, Tychele N Turner, et al.
Cell Reports
|
November 19, 2023
Ion binding with charge inversion combined with screening modulates DEAD box helicase phase transitions
Michael D Crabtree, Jack Holland, Arvind S Pillai, et al.
Science (New York, N.Y.)
|
June 2, 2007
Imaging the surface of Altair
John D Monnier, M Zhao, E Pedretti, et al.
Annals of Clinical and Translational Neurology
|
March 31, 2023
Quantitative determination of SLC2A1 variant functional effects in GLUT1 deficiency syndrome
Naeimeh Tayebi, Brian Leon-Ricardo, Kevin McCall, et al.
Genome Biology and Evolution
|
February 1, 2024
The Impact of Patterns in Linkage Disequilibrium and Sequencing Quality on the Imprint of Balancing Selection
Tristan J Hayeck, Yang Li, Timothy L Mosbruger, et al.
Page
of 56
Search research articles
Search
Showing results (511-520 of 559) with videos related to
Sort By:
Page
of 56
HGG Advances
|
January 20, 2022
From karyotypes to precision genomics in 9p deletion and duplication syndromes
Eleanor I Sams, Jeffrey K Ng, Victoria Tate, et al.
Human Molecular Genetics
|
September 15, 2023
A common single nucleotide variant in the cytokine receptor-like factor-3 (CRLF3) gene causes neuronal deficits in human and mouse cells
Anna F Wilson, Rasha Barakat, Rui Mu, et al.
Genome Research
|
July 24, 2021
Differences in the number of de novo mutations between individuals are due to small family-specific effects and stochasticity
Jakob M Goldmann, Juliet E Hampstead, Wendy S W Wong, et al.
Oncogene
|
January 27, 2010
Integrative molecular profiling of triple negative breast cancers identifies amplicon drivers and potential therapeutic targets
N Turner, M B Lambros, H M Horlings, et al.
Notfall & Rettungsmedizin
|
June 16, 2020
[Education]
C Lott, F Carmona, P Van de Voorde, et al.
The New England Journal of Medicine
|
April 11, 2019
Molecular Genetic Anatomy and Risk Profile of Hirschsprung's Disease
Joseph M Tilghman, Albee Y Ling, Tychele N Turner, et al.
Cell Reports
|
November 19, 2023
Ion binding with charge inversion combined with screening modulates DEAD box helicase phase transitions
Michael D Crabtree, Jack Holland, Arvind S Pillai, et al.
Science (New York, N.Y.)
|
June 2, 2007
Imaging the surface of Altair
John D Monnier, M Zhao, E Pedretti, et al.
Annals of Clinical and Translational Neurology
|
March 31, 2023
Quantitative determination of SLC2A1 variant functional effects in GLUT1 deficiency syndrome
Naeimeh Tayebi, Brian Leon-Ricardo, Kevin McCall, et al.
Genome Biology and Evolution
|
February 1, 2024
The Impact of Patterns in Linkage Disequilibrium and Sequencing Quality on the Imprint of Balancing Selection
Tristan J Hayeck, Yang Li, Timothy L Mosbruger, et al.
Page
of 56