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Familial 18q12.2 deletion supports the role of RNA-binding protein CELF4 in autism spectrum disorders.
Barone, Rita; Fichera, Marco; De Grandi, Mariaclara; Battaglia, Marta; Lo Faro, Valeria; Mattina, Teresa; Rizzo, Renata.
Affiliation
  • Barone R; Department of Clinical and Experimental Medicine, Child Neurology and Psychiatry, University of Catania, Catania, Italy.
  • Fichera M; Department of Biomedical and Biotechnological Sciences, Medical Genetics, University of Catania, Catania, Italy.
  • De Grandi M; Laboratory of Medical Genetics, I.R.C.C.S. Associazione Oasi Maria Santissima, Troina, Italy.
  • Battaglia M; Department of Clinical and Experimental Medicine, Child Neurology and Psychiatry, University of Catania, Catania, Italy.
  • Lo Faro V; Department of Clinical and Experimental Medicine, Child Neurology and Psychiatry, University of Catania, Catania, Italy.
  • Mattina T; Department of Biomedical and Biotechnological Sciences, Medical Genetics, University of Catania, Catania, Italy.
  • Rizzo R; Department of Biomedical and Biotechnological Sciences, Medical Genetics, University of Catania, Catania, Italy.
Am J Med Genet A ; 173(6): 1649-1655, 2017 Jun.
Article in En | MEDLINE | ID: mdl-28407444
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Developmental Disabilities / CELF Proteins / Autism Spectrum Disorder / Intellectual Disability Limits: Adult / Child, preschool / Female / Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2017 Document type: Article Affiliation country: Italy Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Developmental Disabilities / CELF Proteins / Autism Spectrum Disorder / Intellectual Disability Limits: Adult / Child, preschool / Female / Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2017 Document type: Article Affiliation country: Italy Country of publication: United States