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The Journal of Clinical Investigation
|
March 2, 2023
CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis
Nafisa Nuzhat, Kristof Van Schil, Sandra Liakopoulos, et al.
JCI Insight
|
October 5, 2023
Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors
Ghada M H Abdel-Salam, Susanne Hellmuth, Elise Gradhand, et al.
Molecular Psychiatry
|
August 10, 2022
Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits
Aet O'Leary, Noèlia Fernàndez-Castillo, Gabriela Gan, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 43) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 43 results.
The Journal of Clinical Investigation
|
March 2, 2023
CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis
Nafisa Nuzhat, Kristof Van Schil, Sandra Liakopoulos, et al.
JCI Insight
|
October 5, 2023
Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors
Ghada M H Abdel-Salam, Susanne Hellmuth, Elise Gradhand, et al.
Molecular Psychiatry
|
August 10, 2022
Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits
Aet O'Leary, Noèlia Fernàndez-Castillo, Gabriela Gan, et al.
Page
of 5