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Understanding the genetic and epigenetic basis of common variable immunodeficiency disorder through omics approaches.
Li, Jin; Wei, Zhi; Li, Yun R; Maggadottir, S Melkorka; Chang, Xiao; Desai, Akshatha; Hakonarson, Hakon.
Afiliação
  • Li J; Center for Applied Genomics, Children's Hospital of Philadelphia, 3615 Civic Center Boulevard, Philadelphia, PA 19104, USA.
  • Wei Z; Department of Computer Science, New Jersey Institute of Technology, Newark, NJ 07102, USA. Electronic address: zhiwei04@gmail.com.
  • Li YR; Center for Applied Genomics, Children's Hospital of Philadelphia, 3615 Civic Center Boulevard, Philadelphia, PA 19104, USA; Medical Scientist Training Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Maggadottir SM; Department of Immunology, Landspitali University Hospital, Hringbraut (building 14 at Eiriksgata), 101 Reykjavik, Iceland.
  • Chang X; Center for Applied Genomics, Children's Hospital of Philadelphia, 3615 Civic Center Boulevard, Philadelphia, PA 19104, USA.
  • Desai A; Center for Applied Genomics, Children's Hospital of Philadelphia, 3615 Civic Center Boulevard, Philadelphia, PA 19104, USA.
  • Hakonarson H; Center for Applied Genomics, Children's Hospital of Philadelphia, 3615 Civic Center Boulevard, Philadelphia, PA 19104, USA; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA; The Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 1910
Biochim Biophys Acta ; 1860(11 Pt B): 2656-63, 2016 11.
Article em En | MEDLINE | ID: mdl-27316315
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunodeficiência de Variável Comum / Epigênese Genética Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Biochim Biophys Acta Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunodeficiência de Variável Comum / Epigênese Genética Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Biochim Biophys Acta Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos