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Human Molecular Genetics
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June 29, 2023
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration
B H Scammell, C Tchio, Y Song, et al.
Neuromuscular Disorders : NMD
|
January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Haiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.
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of 28
Search research articles
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Showing results (271-280 of 272) with videos related to
Sort By:
Page
of 28
You have reached the last page of results.
This site can display upto 272 results.
Human Molecular Genetics
|
June 29, 2023
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration
B H Scammell, C Tchio, Y Song, et al.
Neuromuscular Disorders : NMD
|
January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Haiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.
Page
of 28