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Brief Report: Sensory Reactivity in Children with Phelan-McDermid Syndrome.
Mieses, A M; Tavassoli, T; Li, E; Soorya, L; Lurie, S; Wang, A T; Siper, P M; Kolevzon, A.
Affiliation
  • Mieses AM; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, Box 1668, One Gustave L. Levy Place, New York, NY, 10029, USA. alexa.mieses@icahn.mssm.edu.
  • Tavassoli T; Seaver Autism Center for Research and Treatment, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, Box 1668, One Gustave L. Levy Place, New York, NY, 10029, USA.
  • Li E; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, Box 1668, One Gustave L. Levy Place, New York, NY, 10029, USA.
  • Soorya L; Department of Psychiatry, Rush University Medical Center, Chicago, IL, USA.
  • Lurie S; Seaver Autism Center for Research and Treatment, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, Box 1668, One Gustave L. Levy Place, New York, NY, 10029, USA.
  • Wang AT; Seaver Autism Center for Research and Treatment, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, Box 1668, One Gustave L. Levy Place, New York, NY, 10029, USA.
  • Siper PM; Seaver Autism Center for Research and Treatment, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, Box 1668, One Gustave L. Levy Place, New York, NY, 10029, USA.
  • Kolevzon A; Seaver Autism Center for Research and Treatment, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, Box 1668, One Gustave L. Levy Place, New York, NY, 10029, USA.
J Autism Dev Disord ; 46(7): 2508-13, 2016 07.
Article de En | MEDLINE | ID: mdl-26914612
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Phénotype / Maladies chromosomiques / Trouble du spectre autistique / Troubles du développement du langage Type d'étude: Diagnostic_studies / Observational_studies / Prognostic_studies Limites: Child / Child, preschool / Female / Humans / Male Langue: En Journal: J Autism Dev Disord Année: 2016 Type de document: Article Pays d'affiliation: États-Unis d'Amérique
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Phénotype / Maladies chromosomiques / Trouble du spectre autistique / Troubles du développement du langage Type d'étude: Diagnostic_studies / Observational_studies / Prognostic_studies Limites: Child / Child, preschool / Female / Humans / Male Langue: En Journal: J Autism Dev Disord Année: 2016 Type de document: Article Pays d'affiliation: États-Unis d'Amérique