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Clinical Validation of Somatic Mutation Detection by the OncoScan CNV Plus Assay.
Smith, Scott C; Farooqi, Midhat S; Gener, Melissa A; Ginn, Kevin; Joyce, Julie M; Bendorf, Tara M; Cooley, Linda D.
Afiliação
  • Smith SC; Department of Pathology & Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri; Department of Pathology & Laboratory Medicine, SUNY Upstate Medical University, Syracuse, New York.
  • Farooqi MS; Department of Pathology & Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri; Department of Pathology & Laboratory Medicine, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri.
  • Gener MA; Department of Pathology & Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri; Department of Pathology & Laboratory Medicine, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri.
  • Ginn K; Department of Pathology & Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri; Department of Pathology & Laboratory Medicine, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri.
  • Joyce JM; Department of Pathology & Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri; Department of Pathology & Laboratory Medicine, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri.
  • Bendorf TM; Department of Pathology & Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri; Department of Pathology & Laboratory Medicine, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri.
  • Cooley LD; Department of Pathology & Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri; Department of Pathology & Laboratory Medicine, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri. Electronic address: lcooley@cmh.edu.
J Mol Diagn ; 23(1): 29-37, 2021 01.
Article em En | MEDLINE | ID: mdl-33080408
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Polimorfismo de Nucleotídeo Único / Análise Serial de Tecidos / Sequenciamento de Nucleotídeos em Larga Escala / Mutação Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Mol Diagn Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Polimorfismo de Nucleotídeo Único / Análise Serial de Tecidos / Sequenciamento de Nucleotídeos em Larga Escala / Mutação Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Mol Diagn Ano de publicação: 2021 Tipo de documento: Article