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Showing results (281-290 of 283) with videos related to

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Human Mutation|March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported IndividualsBobby G Ng, Paulina Sosicka, Satish Agadi, et al.
Nature Metabolism|September 24, 2025
A consensus guide to preclinical indirect calorimetry experimentsAlexander S Banks, David B Allison, Thierry Alquier, et al.
American Journal of Human Genetics|February 17, 2021
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in femalesFrancesca Clementina Radio, Kaifang Pang, Andrea Ciolfi, et al.
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Showing results (281-290 of 283) with videos related to

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Pageof 29
You have reached the last page of results.This site can display upto 283 results.
Human Mutation|March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported IndividualsBobby G Ng, Paulina Sosicka, Satish Agadi, et al.
Nature Metabolism|September 24, 2025
A consensus guide to preclinical indirect calorimetry experimentsAlexander S Banks, David B Allison, Thierry Alquier, et al.
American Journal of Human Genetics|February 17, 2021
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in femalesFrancesca Clementina Radio, Kaifang Pang, Andrea Ciolfi, et al.
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