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Nature Communications
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August 7, 2024
Human genetic structure in Northwest France provides new insights into West European historical demography
Isabel Alves, Joanna Giemza, Michael G B Blum, et al.
Human Mutation
|
March 3, 2019
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders
Christina Zeitz, Christelle Michiels, Marion Neuillé, et al.
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Showing results (21-30 of 22) with videos related to
Sort By:
Page
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This site can display upto 22 results.
Nature Communications
|
August 7, 2024
Human genetic structure in Northwest France provides new insights into West European historical demography
Isabel Alves, Joanna Giemza, Michael G B Blum, et al.
Human Mutation
|
March 3, 2019
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders
Christina Zeitz, Christelle Michiels, Marion Neuillé, et al.
Page
of 3