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Development and Validation of a Next-Generation Sequencing Panel for Syndromic and Nonsyndromic Hearing Loss.
Butz, Malinda; McDonald, Amber; Lundquist, Patrick A; Meyer, Melanie; Harrington, Sean; Kester, Sarah; Stein, Mariam I; Mistry, Nipun A; Zimmerman Zuckerman, Eric; Niu, Zhiyv; Schimmenti, Lisa; Hasadsri, Linda; Boczek, Nicole J.
Afiliação
  • Butz M; Department of Laboratory Medicine and Pathology, Genomics Laboratory, Mayo Clinic, Rochester, MN.
  • McDonald A; Department of Laboratory Medicine and Pathology, Genomics Laboratory, Mayo Clinic, Rochester, MN.
  • Lundquist PA; Department of Laboratory Medicine and Pathology, Genomics Laboratory, Mayo Clinic, Rochester, MN.
  • Meyer M; Department of Laboratory Medicine and Pathology, Genomics Laboratory, Mayo Clinic, Rochester, MN.
  • Harrington S; Department of Laboratory Medicine and Pathology, Genomics Laboratory, Mayo Clinic, Rochester, MN.
  • Kester S; Department of Laboratory Medicine and Pathology, Genomics Laboratory, Mayo Clinic, Rochester, MN.
  • Stein MI; Department of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN.
  • Mistry NA; Department of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN.
  • Zimmerman Zuckerman E; Department of Laboratory Medicine and Pathology, Clinical Genome Sequencing Laboratory, Mayo Clinic, Rochester, MN.
  • Niu Z; Department of Laboratory Medicine and Pathology, Genomics Laboratory, Mayo Clinic, Rochester, MN.
  • Schimmenti L; Department of Laboratory Medicine and Pathology, Clinical Genome Sequencing Laboratory, Mayo Clinic, Rochester, MN.
  • Hasadsri L; Department of Clinical Genomics, Mayo Clinic, Rochester, MN.
  • Boczek NJ; Department of Clinical Genomics, Mayo Clinic, Rochester, MN.
J Appl Lab Med ; 5(3): 467-479, 2020 05 01.
Article em En | MEDLINE | ID: mdl-32445360

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Predisposição Genética para Doença / Sequenciamento de Nucleotídeos em Larga Escala / Perda Auditiva Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Predisposição Genética para Doença / Sequenciamento de Nucleotídeos em Larga Escala / Perda Auditiva Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article