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The Journal of Molecular Diagnostics : JMD|January 1, 2008
A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populationsFlora Tassone, Ruiqin Pan, Khaled Amiri, et al.Journal of Genetic Counseling|August 3, 2015
Attitudes Toward Genetic Testing for Celiac DiseaseAbhik Roy, Michele Pallai, Benjamin Lebwohl, et al.Journal of Autism and Developmental Disorders|October 13, 2006
Autism spectrum phenotype in males and females with fragile X full mutation and premutationSally Clifford, Cheryl Dissanayake, Quang M Bui, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 10, 2018
Venous thromboembolism laboratory testing (factor V Leiden and factor II c.*97G>A), 2018 update: a technical standard of the American College of Medical Genetics and Genomics (ACMG)Shulin Zhang, Annette K Taylor, Xuan Huang, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|December 12, 2002
Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile x males and females assessed by robust pedigree analysisDanuta Z Loesch, Richard M Huggins, Quang M Bui, et al.Clinical Pharmacology and Therapeutics|June 8, 2021
Moving Pharmacogenetics Into Practice: It's All About the Evidence!Jasmine A Luzum, Natasha Petry, Annette K Taylor, et al.Plos One|April 16, 2014
Lack of serologic evidence to link IgA nephropathy with celiac disease or immune reactivity to glutenSina Moeller, Pietro A Canetta, Annette K Taylor, et al.Neuropsychology|November 6, 2003
Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile XDanuta Z Loesch, Quang M Bui, Jim Grigsby, et al.Neuroscience and Biobehavioral Reviews|November 14, 2006
Molecular and cognitive predictors of the continuum of autistic behaviours in fragile XDanuta Z Loesch, Quang M Bui, Cheryl Dissanayake, et al.Molecular Psychiatry|December 12, 2018
Common-variant associations with fragile X syndromeJames J Crowley, Jin Szatkiewicz, Anna K Kähler, et al.Pageof 2