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Behavioral characterization of dup15q syndrome: Toward meaningful endpoints for clinical trials.
DiStefano, Charlotte; Wilson, Rujuta B; Hyde, Carly; Cook, Edwin H; Thibert, Ronald L; Reiter, Lawrence T; Vogel-Farley, Vanessa; Hipp, Joerg; Jeste, Shafali.
Affiliation
  • DiStefano C; Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California.
  • Wilson RB; Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California.
  • Hyde C; Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California.
  • Cook EH; Department of Psychiatry, University of Illinois at Chicago, Chicago, Illinois.
  • Thibert RL; Department of Neurology, Department of Pediatrics, Massachusetts General Hospital, Boston, Massachusetts.
  • Reiter LT; Department of Neurology, Pediatrics, Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, Tennessee.
  • Vogel-Farley V; Dup15q Alliance, Highland Park, Illinois.
  • Hipp J; Roche Pharma Research and Early Development, Neuroscience, Ophthalmology and Rare Diseases, Roche Innovation Center, Basel, Switzerland.
  • Jeste S; Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California.
Am J Med Genet A ; 182(1): 71-84, 2020 01.
Article in En | MEDLINE | ID: mdl-31654560
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / DNA Copy Number Variations / Autism Spectrum Disorder / Intellectual Disability Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / DNA Copy Number Variations / Autism Spectrum Disorder / Intellectual Disability Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Country of publication: