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American Journal of Ophthalmology|July 4, 2002
Discordant pursuit asymmetry and esotropia in monozygous twinsPradeep Sharma, Arthur L Rosenbaum, Terre Vives, et al.American Journal of Medical Genetics. Part A|July 1, 2021
Central 22q11.2 deletion (LCR22 B-D) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndromeIsabella Lin, Yalda Afshar, Jeffrey Goldstein, et al.Molecular Genetics and Metabolism|March 27, 2002
Cloning and characterization of human agmatinaseRamaswamy K Iyer, Ho K Kim, Rosemarie W Tsoa, et al.Molecular Genetics and Metabolism|March 31, 2004
Arginases I and II: do their functions overlap?Stephen D Cederbaum, Hong Yu, Wayne W Grody, et al.The Prostate|July 30, 2008
Disruption of arginase II alters prostate tumor formation in TRAMP miceShannon M Mumenthaler, Nora Rozengurt, Justin C Livesay, et al.Journal of Genetic Counseling|October 24, 2007
Ethnic differences in parental perceptions of genetic testing for deaf infantsChristina G S Palmer, Ariadna Martinez, Michelle Fox, et al.Nucleic Acids Research|June 13, 2002
An electrochemical detection scheme for identification of single nucleotide polymorphisms using hairpin-forming probesTony Jun Huang, Minghsun Liu, Linda D Knight, et al.Molecular Genetics & Genomic Medicine|November 9, 2019
Confidential genetic testing and electronic health records: A survey of current practices among Huntington disease testing centersCeleste C Eno, Stacey K Barton, Naghmeh Dorrani, et al.Plos One|May 28, 2010
Arginine metabolism by macrophages promotes cardiac and muscle fibrosis in mdx muscular dystrophyMichelle Wehling-Henricks, Maria C Jordan, Tomomi Gotoh, et al.Journal of Molecular Neuroscience : MN|December 25, 2016
A Sodium Channel Myotonia Presenting with Intermittent Dysphagia as a Manifestation of a Rare SCN4A VariantJihane N Benhammou, Jennifer Phan, Hane Lee, et al.Pageof 11