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Biorxiv : the Preprint Server for Biology
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February 15, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseases
Shu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics
|
February 22, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseases
Shu Wen, Meng Wang, Xinye Qian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 20, 2020
Ceramide synthase TLCD3B is a novel gene associated with human recessive retinal dystrophy
Renae Elaine Bertrand, Jun Wang, Kaitlyn H Xiong, et al.
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of 5
Search research articles
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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.
Biorxiv : the Preprint Server for Biology
|
February 15, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseases
Shu Wen, Meng Wang, Xinye Qian, et al.
Human Molecular Genetics
|
February 22, 2023
Systematic assessment of the contribution of structural variants to inherited retinal diseases
Shu Wen, Meng Wang, Xinye Qian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 20, 2020
Ceramide synthase TLCD3B is a novel gene associated with human recessive retinal dystrophy
Renae Elaine Bertrand, Jun Wang, Kaitlyn H Xiong, et al.
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of 5