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Science Bulletin
|
December 10, 2021
Reprogramming of Ovarian Granulosa Cells by YAP1 Leads to Development of High-Grade Cancer with Mesenchymal Lineage and Serous Features
Xiangmin Lv, Chunbo He, Cong Huang, et al.
Human Mutation
|
August 11, 2018
Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar
Erin R Riggs, Tristan Nelson, Andrew Merz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
Erin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Circulation
|
June 21, 2019
Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants
Christopher M Haggerty, Scott M Damrauer, Michael G Levin, et al.
American Journal of Human Genetics
|
November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
Daniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Nature Neuroscience
|
April 18, 2023
Author Correction: A consensus protocol for functional connectivity analysis in the rat brain
Joanes Grandjean, Gabriel Desrosiers-Gregoire, Cynthia Anckaerts, et al.
Nature Neuroscience
|
March 27, 2023
A consensus protocol for functional connectivity analysis in the rat brain
Joanes Grandjean, Gabriel Desrosiers-Gregoire, Cynthia Anckaerts, et al.
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Search research articles
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Showing results (301-310 of 307) with videos related to
Sort By:
Page
of 31
You have reached the last page of results.
This site can display upto 307 results.
Science Bulletin
|
December 10, 2021
Reprogramming of Ovarian Granulosa Cells by YAP1 Leads to Development of High-Grade Cancer with Mesenchymal Lineage and Serous Features
Xiangmin Lv, Chunbo He, Cong Huang, et al.
Human Mutation
|
August 11, 2018
Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar
Erin R Riggs, Tristan Nelson, Andrew Merz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
Erin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Circulation
|
June 21, 2019
Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants
Christopher M Haggerty, Scott M Damrauer, Michael G Levin, et al.
American Journal of Human Genetics
|
November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
Daniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Nature Neuroscience
|
April 18, 2023
Author Correction: A consensus protocol for functional connectivity analysis in the rat brain
Joanes Grandjean, Gabriel Desrosiers-Gregoire, Cynthia Anckaerts, et al.
Nature Neuroscience
|
March 27, 2023
A consensus protocol for functional connectivity analysis in the rat brain
Joanes Grandjean, Gabriel Desrosiers-Gregoire, Cynthia Anckaerts, et al.
Page
of 31