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Observable Symptoms of Anxiety in Individuals with Fragile X Syndrome: Parent and Caregiver Perspectives.
Lozano, Reymundo; Thompson, Talia; Dixon-Weber, Jayne; Erickson, Craig A; Berry-Kravis, Elizabeth; Williams, Sara; Smith, Elizabeth; Frazier, Jean A; Rosselot, Hilary; Farmer, Cristan; Hessl, David.
Afiliación
  • Lozano R; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Thompson T; Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Dixon-Weber J; Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA.
  • Erickson CA; National Fragile X Foundation, Washington, DC 20005, USA.
  • Berry-Kravis E; Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
  • Williams S; Department of Pediatrics, Rush University Medical Center, Chicago, IL 60612, USA.
  • Smith E; Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
  • Frazier JA; Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
  • Rosselot H; Department of Psychiatry, Chan Medical School, University of Massachusetts, Worcester, MA 01655, USA.
  • Farmer C; National Fragile X Foundation, Washington, DC 20005, USA.
  • Hessl D; Neurodevelopmental and Behavioral Phenotyping Service, National Institute of Mental Health, Bethesda, MD 20892, USA.
Genes (Basel) ; 13(9)2022 09 16.
Article en En | MEDLINE | ID: mdl-36140827
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article