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Expanding the clinical history associated with syndromic Klippel-Feil: A unique case of comorbidity with medulloblastoma.
Schieffer, Kathleen M; Varga, Elizabeth; Miller, Katherine E; Agarwal, Vibhuti; Koboldt, Daniel C; Brennan, Patrick; Kelly, Benjamin; Dave-Wala, Ashita; Pierson, Christopher R; Finlay, Jonathan L; AbdelBaki, Mohamed S; White, Peter; Magrini, Vincent; Wilson, Richard K; Mardis, Elaine R; Cottrell, Catherine E.
Afiliação
  • Schieffer KM; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA. Electronic address: Kathleen.Schieffer@nationwidechildrens.org.
  • Varga E; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA; Division of Hematology, Oncology and Bone Marrow Transplant, Nationwide Children's Hospital, Columbus, OH, USA.
  • Miller KE; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA.
  • Agarwal V; Division of Hematology, Oncology and Bone Marrow Transplant, Nationwide Children's Hospital, Columbus, OH, USA.
  • Koboldt DC; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA.
  • Brennan P; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA.
  • Kelly B; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA.
  • Dave-Wala A; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA.
  • Pierson CR; Department of Pathology and Laboratory Medicine, Nationwide Children's Hospital, Columbus, OH, USA; Department of Biomedical Education and Anatomy, The Ohio State University, Columbus, OH, USA.
  • Finlay JL; Division of Hematology, Oncology and Bone Marrow Transplant, Nationwide Children's Hospital, Columbus, OH, USA; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA.
  • AbdelBaki MS; Division of Hematology, Oncology and Bone Marrow Transplant, Nationwide Children's Hospital, Columbus, OH, USA.
  • White P; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA.
  • Magrini V; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA.
  • Wilson RK; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA.
  • Mardis ER; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA.
  • Cottrell CE; Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, USA; Department of Pathology, The Ohio State University College of Medicine, Columbus, OH, USA.
Eur J Med Genet ; 62(8): 103701, 2019 Aug.
Article em En | MEDLINE | ID: mdl-31195167
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Miosinas / Proteínas Supressoras de Tumor / Sequenciamento do Exoma / Síndrome de Klippel-Feil / Meduloblastoma Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Humans / Male Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Miosinas / Proteínas Supressoras de Tumor / Sequenciamento do Exoma / Síndrome de Klippel-Feil / Meduloblastoma Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Humans / Male Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article