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Descriptive analysis of seizures and comorbidities associated with fragile X syndrome.
Albizua, Igor; Charen, Krista; Shubeck, Lisa; Talboy, Amy; Berry-Kravis, Elizabeth; Kaufmann, Walter E; Stallworth, Jennifer L; Drazba, Katy T; Erickson, Craig A; Sweeney, John A; Tartaglia, Nicole; Warren, Steven F; Hagerman, Randi; Sherman, Stephanie L; Warren, Stephen T; Jin, Peng; Allen, Emily G.
Afiliación
  • Albizua I; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Charen K; Department of Pathology, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Shubeck L; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Talboy A; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Berry-Kravis E; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Kaufmann WE; Department of Pediatrics, Neurological Sciences, Biochemistry, Rush University Medical Center, Chicago, Illinois, USA.
  • Stallworth JL; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Drazba KT; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Erickson CA; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Sweeney JA; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Tartaglia N; Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Warren SF; Department of Psychiatry, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Hagerman R; Department of Pediatrics, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, Colorado, USA.
  • Sherman SL; Department of Speech-Language-Hearing: Sciences & Disorders, The University of Kansas, Lawrence, Kansas, USA.
  • Warren ST; Department of Pediatrics, University of California Davis MIND Institute, Sacramento, California, USA.
  • Jin P; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Allen EG; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, USA.
Mol Genet Genomic Med ; 10(8): e2001, 2022 08.
Article en En | MEDLINE | ID: mdl-35852003
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Prolapso de la Válvula Mitral / Trastorno del Espectro Autista / Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Prolapso de la Válvula Mitral / Trastorno del Espectro Autista / Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article