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Novel parent-of-origin-specific differentially methylated loci on chromosome 16.
Schulze, Katharina V; Szafranski, Przemyslaw; Lesmana, Harry; Hopkin, Robert J; Hamvas, Aaron; Wambach, Jennifer A; Shinawi, Marwan; Zapata, Gladys; Carvalho, Claudia M B; Liu, Qian; Karolak, Justyna A; Lupski, James R; Hanchard, Neil A; Stankiewicz, Pawel.
Afiliação
  • Schulze KV; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Szafranski P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Lesmana H; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
  • Hopkin RJ; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
  • Hamvas A; Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Wambach JA; Division of Newborn Medicine, Edward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA.
  • Shinawi M; Division of Genetics and Genomic Medicine, Edward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA.
  • Zapata G; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Carvalho CMB; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Liu Q; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Karolak JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Hanchard NA; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Stankiewicz P; Texas Children's Hospital, Houston, TX, USA.
Clin Epigenetics ; 11(1): 60, 2019 04 08.
Article em En | MEDLINE | ID: mdl-30961659
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Metilação de DNA / Polimorfismo de Nucleotídeo Único / Dissomia Uniparental Limite: Female / Humans / Male Idioma: En Revista: Clin Epigenetics Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Alemanha
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Metilação de DNA / Polimorfismo de Nucleotídeo Único / Dissomia Uniparental Limite: Female / Humans / Male Idioma: En Revista: Clin Epigenetics Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Alemanha