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Nature Communications
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February 5, 2022
Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene
Gudny A Arnadottir, Asmundur Oddsson, Brynjar O Jensson, et al.
American Journal of Human Genetics
|
July 8, 2023
Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration
Annalisa Vetro, Cristiana Pelorosso, Simona Balestrini, et al.
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Search research articles
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Showing results (11-20 of 12) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 12 results.
Nature Communications
|
February 5, 2022
Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene
Gudny A Arnadottir, Asmundur Oddsson, Brynjar O Jensson, et al.
American Journal of Human Genetics
|
July 8, 2023
Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration
Annalisa Vetro, Cristiana Pelorosso, Simona Balestrini, et al.
Page
of 2