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Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes.
Tucker, Tracy; Zahir, Farah R; Griffith, Malachi; Delaney, Allen; Chai, David; Tsang, Erica; Lemyre, Emmanuelle; Dobrzeniecka, Sylvia; Marra, Marco; Eydoux, Patrice; Langlois, Sylvie; Hamdan, Fadi F; Michaud, Jacques L; Friedman, Jan M.
Afiliação
  • Tucker T; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Zahir FR; 1] Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada [2] Canada's Michael Smith Genome Sciences Centre, Vancouver, British Columbia, Canada.
  • Griffith M; Canada's Michael Smith Genome Sciences Centre, Vancouver, British Columbia, Canada.
  • Delaney A; Canada's Michael Smith Genome Sciences Centre, Vancouver, British Columbia, Canada.
  • Chai D; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Tsang E; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Lemyre E; CHU Sainte-Justine Research Center, Montréal, Quebec, Canada.
  • Dobrzeniecka S; CHU Sainte-Justine Research Center, Montréal, Quebec, Canada.
  • Marra M; Canada's Michael Smith Genome Sciences Centre, Vancouver, British Columbia, Canada.
  • Eydoux P; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Langlois S; 1] Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada [2] Provincial Medical Genetics Programme, Children's & Women's Health Centre of British Columbia, Vancouver, British Columbia, Canada.
  • Hamdan FF; CHU Sainte-Justine Research Center, Montréal, Quebec, Canada.
  • Michaud JL; CHU Sainte-Justine Research Center, Montréal, Quebec, Canada.
  • Friedman JM; 1] Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada [2] Child & Family Research Institute, Vancouver, British Columbia, Canada.
Eur J Hum Genet ; 22(6): 792-800, 2014 Jun.
Article em En | MEDLINE | ID: mdl-24253858
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Éxons / Predisposição Genética para Doença / Análise de Sequência com Séries de Oligonucleotídeos / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Female / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Éxons / Predisposição Genética para Doença / Análise de Sequência com Séries de Oligonucleotídeos / Deficiência Intelectual Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Female / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article