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Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder.
Chapman, N H; Bernier, R A; Webb, S J; Munson, J; Blue, E M; Chen, D-H; Heigham, E; Raskind, W H; Wijsman, Ellen M.
Affiliation
  • Chapman NH; Division of Medical Genetics, Department of Medicine, University of Washington, Box 359460, Seattle, WA, 98195, USA.
  • Bernier RA; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, 98195, USA.
  • Webb SJ; Center on Human Development and Disability, University of Washington, Seattle, WA, 98195, USA.
  • Munson J; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, 98195, USA.
  • Blue EM; Center on Human Development and Disability, University of Washington, Seattle, WA, 98195, USA.
  • Chen DH; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, 98195, USA.
  • Heigham E; Center on Human Development and Disability, University of Washington, Seattle, WA, 98195, USA.
  • Raskind WH; Division of Medical Genetics, Department of Medicine, University of Washington, Box 359460, Seattle, WA, 98195, USA.
  • Wijsman EM; Department of Neurology, University of Washington, Seattle, WA, 98195, USA.
Hum Genet ; 137(10): 807-815, 2018 Oct.
Article in En | MEDLINE | ID: mdl-30276537
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Repressor Proteins / Haplotypes / Mutation, Missense / Eye Proteins / Genetic Loci / Autism Spectrum Disorder Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Hum Genet Year: 2018 Type: Article Affiliation country: United States
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Repressor Proteins / Haplotypes / Mutation, Missense / Eye Proteins / Genetic Loci / Autism Spectrum Disorder Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Hum Genet Year: 2018 Type: Article Affiliation country: United States