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The Application of Clinical Genetics|February 3, 2021
Spinal Muscular Atrophy: Mutations, Testing, and Clinical RelevanceMelissa C Keinath, Devin E Prior, Thomas W Prior
Eneurologicalsci|November 20, 2018
Comparison of costs and outcomes of patients presenting with a rare brainstem syndromeDevin E Prior, Vijay Renga
Genome Research|June 7, 2015
The sea lamprey meiotic map improves resolution of ancient vertebrate genome duplicationsJeramiah J Smith, Melissa C Keinath
Journal of Child Neurology|January 20, 2021
Congenital Myasthenic Syndrome From a Single Center: Phenotypic and Genotypic featuresDevin E Prior, Partha S Ghosh
Obstetrics and Gynecology Clinics of North America|May 25, 2010
Spinal muscular atrophy: newborn and carrier screeningThomas W Prior
Journal of Child Neurology|September 1, 2007
Spinal muscular atrophy diagnosticsThomas W Prior
Genome Medicine|December 5, 2014
Next-generation carrier screening: are we ready?Thomas W Prior
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2010
Perspectives and diagnostic considerations in spinal muscular atrophyThomas W Prior
Current Opinion in Pediatrics|September 11, 2010
Spinal muscular atrophy: a time for screeningThomas W Prior
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 24, 2009
Technical standards and guidelines for myotonic dystrophy type 1 testingThomas W Prior,
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