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Muscle & Nerve|September 26, 2008
Recessive CLCN1 mutation presenting as Thomsen diseaseJudy Thomas, Jack Tarleton, Steven K BakerJournal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 4, 2008
Extraocular muscle hypertrophy in myotonia congenitaBradley Wakeman, Deepti Babu, Jack Tarleton, et al.American Journal of Medical Genetics. Part A|May 27, 2010
The course of cognitive-behavioral development in children with the FMR1 mutation, Williams-Beuren syndrome, and neurofibromatosis type 1: The effect of genderGene S Fisch, Nancy Carpenter, Patricia N Howard-Peebles, et al.American Journal on Intellectual and Developmental Disabilities|April 21, 2012
Developmental trajectories in syndromes with intellectual disability, with a focus on Wolf-Hirschhorn and its cognitive-behavioral profileGene S Fisch, Nancy Carpenter, Patricia N Howard-Peebles, et al.American Journal of Medical Genetics. Part A|September 14, 2007
Studies of age-correlated features of cognitive-behavioral development in children and adolescents with genetic disordersGene S Fisch, Nancy Carpenter, Patricia N Howard-Peebles, et al.The Journal of Molecular Diagnostics : JMD|May 18, 2013
Development of a genomic DNA reference material panel for myotonic dystrophy type 1 (DM1) genetic testingLisa Kalman, Jack Tarleton, Monica Hitch, et al.The Journal of Molecular Diagnostics : JMD|April 11, 2009
Development of genomic reference materials for cystic fibrosis genetic testingVictoria M Pratt, Michele Caggana, Christina Bridges, et al.The Journal of Molecular Diagnostics : JMD|March 1, 2011
Quality assurance for Duchenne and Becker muscular dystrophy genetic testing: development of a genomic DNA reference material panelLisa Kalman, Jay Leonard, Norman Gerry, et al.Pageof 1