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American Journal of Medical Genetics. Part A|July 29, 2003
Screening of patients with craniosynostosis: molecular strategyKathy Chun, Ahmad S Teebi, Cyrus Azimi, et al.Clinical Leadership & Management Review : the Journal of CLMA|February 19, 2004
Providing information at the point of care: educational diagnostic reports from a genetic testing service providerLisa M Goos, Irwin Silverman, Leslie Steele, et al.Human Molecular Genetics|October 1, 1996
Expression of the dystrophin isoform Dp71 in differentiating human fetal myogenic culturesC N Tennyson, G Y Dally, P N Ray, et al.Neuromuscular Disorders : NMD|February 24, 2009
Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin geneBerivan Baskin, Brenda Banwell, Reem Al Khater, et al.Journal of Psychiatric Practice|November 20, 2012
Undergraduate students' perceptions of practicing psychiatristsMichael W Firmin, Richard A Wantz, Ellen F Geib, et al.The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|February 25, 2020
Transgender Youth's Disclosure of Gender Identity to Providers Outside of Specialized Gender CentersGina M Sequeira, Kristin N Ray, Elizabeth Miller, et al.The Journal of the Association of Physicians of India|March 7, 2006
HIV infection with myasthenia gravisS P Gorthi, S Shankar, S Johri, et al.Pediatrics|December 1, 2023
Accuracy of a Single Financial Security Question to Screen for Social NeedsJanel Hanmer, Kristin N Ray, Kelsey Schweiberger, et al.Molecular and Cellular Biology|May 1, 1986
Molecular cloning of cDNA for rat argininosuccinate lyase and its expression in rat hepatoma cell linesM A Lambert, L R Simard, P N Ray, et al.Neurology|September 25, 1998
Congenital cytoplasmic body myopathy with survival motor neuron gene deletion or Werdnig-Hoffmann diseaseJ Vajsar, T Balslev, P N Ray, et al.Pageof 56