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Journal of Neuropathology and Experimental Neurology|October 6, 2006
Limb-girdle muscular dystrophy in the United StatesSteven A Moore, Christopher J Shilling, Steven Westra, et al.Brain : a Journal of Neurology|February 16, 2013
Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathiesAnn E Davidson, Fazeel M Siddiqui, Michael A Lopez, et al.Metabolomics : Official Journal of the Metabolomic Society|January 20, 2015
Molecular phenotyping of a UK population: defining the human serum metabolomeWarwick B Dunn, Wanchang Lin, David Broadhurst, et al.Analytical Chemistry|October 23, 2019
International Ring Trial of a High Resolution Targeted Metabolomics and Lipidomics Platform for Serum and Plasma AnalysisJ Will Thompson, Kendra J Adams, Jerzy Adamski, et al.Human Mutation|April 3, 2014
Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathiesMinttu Marttila, Vilma-Lotta Lehtokari, Steven Marston, et al.Journal of Medical Genetics|July 14, 2012
Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic HedgehogBenjamin D Solomon, Kelly A Bear, Adrian Wyllie, et al.Ebiomedicine|January 23, 2026
Endocrine and metabolic determinants of cardiometabolic risk in mild autonomous cortisol secretionAlessandro Prete, Lida Abdi, Marco Canducci, et al.Pageof 12