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NPJ Genomic Medicine
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April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypes
Ryan E Schmidt, Amy E Pohodich, David Birch, et al.
Neuron
|
May 1, 2021
Brainhack: Developing a culture of open, inclusive, community-driven neuroscience
Rémi Gau, Stephanie Noble, Katja Heuer, et al.
Annals of the Rheumatic Diseases
|
July 22, 2022
Gain-of-function mutations in <i>ALPK1</i> cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome
Christina Torres Kozycki, Shilpa Kodati, Laryssa Huryn, et al.
Molecular Ecology Resources
|
May 14, 2011
Permanent Genetic Resources added to Molecular Ecology Resources Database 1 April 2010 - 31 May 2010
, K Andree, Jan Axtner, et al.
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of 86
Search research articles
Search
Showing results (851-860 of 854) with videos related to
Sort By:
Page
of 86
You have reached the last page of results.
This site can display upto 854 results.
NPJ Genomic Medicine
|
April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypes
Ryan E Schmidt, Amy E Pohodich, David Birch, et al.
Neuron
|
May 1, 2021
Brainhack: Developing a culture of open, inclusive, community-driven neuroscience
Rémi Gau, Stephanie Noble, Katja Heuer, et al.
Annals of the Rheumatic Diseases
|
July 22, 2022
Gain-of-function mutations in <i>ALPK1</i> cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome
Christina Torres Kozycki, Shilpa Kodati, Laryssa Huryn, et al.
Molecular Ecology Resources
|
May 14, 2011
Permanent Genetic Resources added to Molecular Ecology Resources Database 1 April 2010 - 31 May 2010
, K Andree, Jan Axtner, et al.
Page
of 86