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Moving away from one disease at a time: Screening, trial design, and regulatory implications of novel platform technologies.
Lekstrom-Himes, Julie; Brooks, P J; Koeberl, Dwight D; Brower, Amy; Goldenberg, Aaron; Green, Robert C; Morris, Jill A; Orsini, Joseph J; Yu, Timothy W; Augustine, Erika F.
Afiliação
  • Lekstrom-Himes J; Takeda, Cambridge, Massachusetts, USA.
  • Brooks PJ; Division of Rare Diseases Research Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland, USA.
  • Koeberl DD; Division of Medical Genetics, Department of Pediatrics, Duke University School of Medicine, Durham, North Carolina, USA.
  • Brower A; American College of Medical Genetics and Genomics, Bethesda, Maryland, USA.
  • Goldenberg A; Department of Bioethics, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
  • Green RC; Mass General Brigham, Broad Institute, Ariadne Labs and Harvard Medical School, Boston, MA, USA.
  • Morris JA; National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
  • Orsini JJ; Wadsworth Center, New York State Department of Health, Albany, New York, USA.
  • Yu TW; Division of Genetics and Genomics, Harvard Medical School, Boston, Massachusetts, USA.
  • Augustine EF; Department of Neurology and Neurodevelopmental Medicine, Kennedy Krieger Institute, Baltimore, Maryland, USA.
Am J Med Genet C Semin Med Genet ; 193(1): 30-43, 2023 03.
Article em En | MEDLINE | ID: mdl-36738469

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Raras / Edição de Genes Tipo de estudo: Diagnostic_studies / Guideline / Screening_studies Limite: Humans / Newborn Idioma: En Revista: Am J Med Genet C Semin Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Raras / Edição de Genes Tipo de estudo: Diagnostic_studies / Guideline / Screening_studies Limite: Humans / Newborn Idioma: En Revista: Am J Med Genet C Semin Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos
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