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Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome.
Guo, Tingwei; Chung, Jonathan H; Wang, Tao; McDonald-McGinn, Donna M; Kates, Wendy R; Hawula, Wanda; Coleman, Karlene; Zackai, Elaine; Emanuel, Beverly S; Morrow, Bernice E.
Afiliação
  • Guo T; Department of Genetics, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA.
  • Chung JH; Department of Genetics, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA.
  • Wang T; Department of Epidemiology & Population Health, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA.
  • McDonald-McGinn DM; Division of Human Genetics, The Children's Hospital of Philadelphia, and Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Kates WR; Department of Psychiatry and Behavioral Sciences, and Program in Neuroscience, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
  • Hawula W; Department of Genetics, Polish Mother's Memorial Hospital - Research Institute, Lódz 93-338, Poland.
  • Coleman K; Marcus Autism Center, Children's Healthcare of Atlanta, Atlanta, GA 30329, USA.
  • Zackai E; Division of Human Genetics, The Children's Hospital of Philadelphia, and Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Emanuel BS; Division of Human Genetics, The Children's Hospital of Philadelphia, and Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Morrow BE; Department of Genetics, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY 10461, USA. Electronic address: bernice.morrow@einstein.yu.edu.
Am J Hum Genet ; 97(6): 869-77, 2015 Dec 03.
Article em En | MEDLINE | ID: mdl-26608785
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxirredutases N-Desmetilantes / Fatores de Transcrição / Proteínas Nucleares / Histonas / Síndrome de DiGeorge / Proteínas de Ligação a DNA / Histona Desmetilases com o Domínio Jumonji / Cardiopatias Congênitas Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxirredutases N-Desmetilantes / Fatores de Transcrição / Proteínas Nucleares / Histonas / Síndrome de DiGeorge / Proteínas de Ligação a DNA / Histona Desmetilases com o Domínio Jumonji / Cardiopatias Congênitas Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article