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Human Mutation
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March 25, 2022
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia
Maria Solaki, Britta Baumann, Peggy Reuter, et al.
Nature Genetics
|
August 23, 2016
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy, Sayantan Das, Warren Kretzschmar, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa
Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova, et al.
Nature Genetics
|
January 9, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova, et al.
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of 6
Search research articles
Search
Showing results (51-60 of 54) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 54 results.
Human Mutation
|
March 25, 2022
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia
Maria Solaki, Britta Baumann, Peggy Reuter, et al.
Nature Genetics
|
August 23, 2016
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy, Sayantan Das, Warren Kretzschmar, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa
Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova, et al.
Nature Genetics
|
January 9, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova, et al.
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of 6