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Implications of COMT long-range interactions on the phenotypic variability of 22q11.2 deletion syndrome.
Zeitz, Michael J; Lerner, Paula P; Ay, Ferhat; Van Nostrand, Eric; Heidmann, Julia D; Noble, William S; Hoffman, Andrew R.
Afiliação
  • Zeitz MJ; Veterans Affairs Palo Alto Health Care System; Stanford University Medical School; Palo Alto, CA USA; Department of Genome Sciences; University of Washington; Seattle, WA USA; Department of Genetics and Department of Developmental Biology; Stanford University Medical Center; Stanford, CA USA; Depart
  • Lerner PP; Veterans Affairs Palo Alto Health Care System; Stanford University Medical School; Palo Alto, CA USA.
  • Ay F; Department of Genome Sciences; University of Washington; Seattle, WA USA.
  • Van Nostrand E; Department of Genetics and Department of Developmental Biology; Stanford University Medical Center; Stanford, CA USA.
  • Heidmann JD; Veterans Affairs Palo Alto Health Care System; Stanford University Medical School; Palo Alto, CA USA.
  • Noble WS; Department of Genome Sciences; University of Washington; Seattle, WA USA; Department of Computer Science and Engineering; University of Washington; Seattle, WA USA.
  • Hoffman AR; Veterans Affairs Palo Alto Health Care System; Stanford University Medical School; Palo Alto, CA USA.
Nucleus ; 4(6): 487-93, 2013.
Article em En | MEDLINE | ID: mdl-24448439
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Variação Genética / Catecol O-Metiltransferase / Deleção Cromossômica / Síndrome de DiGeorge Idioma: En Ano de publicação: 2013 Tipo de documento: Article
Texto completo
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XML
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Variação Genética / Catecol O-Metiltransferase / Deleção Cromossômica / Síndrome de DiGeorge Idioma: En Ano de publicação: 2013 Tipo de documento: Article