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Pediatrics|December 15, 2010
Serum transaminase levels in boys with Duchenne and Becker muscular dystrophyHugh J McMillan, Matt Gregas, Basil T Darras, et al.Journal of Neuro-Oncology|January 1, 1994
Clonal analysis of human astrocytomasR P Morse, B T Darras, Z Ye, et al.American Journal of Medical Genetics|June 28, 2001
Exclusion of growth factor gene mutations as a common cause of Sotos syndromeA E Lin, Q Liu, G B Mannheim, et al.American Journal of Human Genetics|August 1, 1989
Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13U Francke, B T Darras, N F Zander, et al.Journal of Neuro-Oncology|January 1, 1993
Aggressive oligodendroglioma predicted by chromosome 10 restriction fragment length polymorphism analysis. Case studyJ K Wu, R D Folkerth, Z Ye, et al.Brain & Development|July 1, 1992
A search for X-chromosome uniparental disomy and DNA rearrangements in the Rett syndromeM J Rivkin, Z Ye, G B Mannheim, et al.Pediatric Neurology|July 9, 2010
Electrophysiologic evidence for anterior horn cell disease in amyoplasiaJohn N Gaitanis, Hugh J McMillan, Allan Wu, et al.Neurology|July 13, 2012
Machine learning algorithms to classify spinal muscular atrophy subtypesTuhin Srivastava, Basil T Darras, Jim S Wu, et al.Genomics|May 1, 1991
Structure of the human cytochrome c oxidase subunit Vb gene and chromosomal mapping of the coding gene and of seven pseudogenesM I Lomax, C L Hsieh, B T Darras, et al.American Journal of Speech-Language Pathology|April 6, 2021
Dysphagia Phenotypes in Spinal Muscular Atrophy: The Past, Present, and Promise for the FutureKatlyn Elizabeth McGrattan, Robert J Graham, Christine J DiDonato, et al.Pageof 110