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Estimation of copy number aberrations: Comparison of exome sequencing data with SNP microarrays identifies homozygous deletions of 19q13.2 and CIC in neuroblastoma.
Fransson, Susanne; Östensson, Malin; Djos, Anna; Javanmardi, Niloufar; Kogner, Per; Martinsson, Tommy.
Afiliação
  • Fransson S; Department of Medical and Clinical Genetics, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
  • Östensson M; Department of Medical and Clinical Genetics, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
  • Djos A; Department of Medical and Clinical Genetics, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
  • Javanmardi N; Department of Medical and Clinical Genetics, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
  • Kogner P; Childhood Cancer Research Unit, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
  • Martinsson T; Department of Medical and Clinical Genetics, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Int J Oncol ; 48(3): 1103-16, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26794043
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Cromossomos Humanos Par 19 / Deleção de Genes / Dosagem de Genes / Polimorfismo de Nucleotídeo Único / Neuroblastoma Tipo de estudo: Prognostic_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Cromossomos Humanos Par 19 / Deleção de Genes / Dosagem de Genes / Polimorfismo de Nucleotídeo Único / Neuroblastoma Tipo de estudo: Prognostic_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article