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Fernando Corrales

Showing results (41-50 of 42) with videos related to

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Orphanet Journal of Rare Diseases|August 21, 2015
Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotesYin-Hsiu Chien, Jose E Abdenur, Federico Baronio, et al.
Nature|December 11, 2024
π-HuB: the proteomic navigator of the human bodyFuchu He, Ruedi Aebersold, Mark S Baker, et al.
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Showing results (41-50 of 42) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 42 results.
Orphanet Journal of Rare Diseases|August 21, 2015
Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotesYin-Hsiu Chien, Jose E Abdenur, Federico Baronio, et al.
Nature|December 11, 2024
π-HuB: the proteomic navigator of the human bodyFuchu He, Ruedi Aebersold, Mark S Baker, et al.
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