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Molecular Genetics and Metabolism|January 16, 2010
Diagnoses of newborns and mothers with carnitine uptake defects through newborn screeningNi-Chung Lee, Nelson Leung-Sang Tang, Yin-Hsiu Chien, et al.
Dalton Transactions (Cambridge, England : 2003)|March 12, 2010
Formation of a homocitrate-free iron-molybdenum cluster on NifEN: implications for the role of homocitrate in nitrogenase assemblyAaron Wolfe Fay, Michael Aaron Blank, Janice Mariko Yoshizawa, et al.
Experimental Biology and Medicine (Maywood, N.J.)|April 25, 2015
Laboratory diagnosis of melioidosis: past, present and futureSusanna K P Lau, Siddharth Sridhar, Chi-Chun Ho, et al.
Plos One|April 8, 2015
Structural and functional roles of glycosylation in fungal laccase from Lentinus spManuel Maestre-Reyna, Wei-Chun Liu, Wen-Yih Jeng, et al.
BMC Medical Genetics|February 28, 2018
Expansion of phenotypic spectrum of MYO15A pathogenic variants to include postlingual onset of progressive partial deafnessMun Young Chang, Chung Lee, Jin Hee Han, et al.
Neurobiology of Aging|December 4, 2018
Genetic variants of PARK genes in Korean patients with early-onset Parkinson's diseaseJinyoung Youn, Chung Lee, Eungseok Oh, et al.
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