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Nature Communications
|
May 8, 2021
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder
Sukhleen Kour, Deepa S Rajan, Tyler R Fortuna, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 4, 2020
Impact of integrated translational research on clinical exome sequencing
Eric W Klee, Margot A Cousin, Filippo Pinto E Vairo, et al.
Biological Psychiatry
|
August 25, 2019
Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling
Brett V Johnson, Raman Kumar, Sabrina Oishi, et al.
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Search research articles
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Showing results (261-270 of 263) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 263 results.
Nature Communications
|
May 8, 2021
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder
Sukhleen Kour, Deepa S Rajan, Tyler R Fortuna, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 4, 2020
Impact of integrated translational research on clinical exome sequencing
Eric W Klee, Margot A Cousin, Filippo Pinto E Vairo, et al.
Biological Psychiatry
|
August 25, 2019
Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling
Brett V Johnson, Raman Kumar, Sabrina Oishi, et al.
Page
of 27