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Clinical outcomes of a genomic screening program for actionable genetic conditions.
Buchanan, Adam H; Lester Kirchner, H; Schwartz, Marci L B; Kelly, Melissa A; Schmidlen, Tara; Jones, Laney K; Hallquist, Miranda L G; Rocha, Heather; Betts, Megan; Schwiter, Rachel; Butry, Loren; Lazzeri, Amanda L; Frisbie, Lauren R; Rahm, Alanna Kulchak; Hao, Jing; Willard, Huntington F; Martin, Christa L; Ledbetter, David H; Williams, Marc S; Sturm, Amy C.
Afiliação
  • Buchanan AH; Genomic Medicine Institute, Geisinger, Danville, PA, USA. ahbuchanan@geisinger.edu.
  • Lester Kirchner H; Department of Population Health Sciences, Geisinger, Danville, PA, USA.
  • Schwartz MLB; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Kelly MA; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Schmidlen T; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Jones LK; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Hallquist MLG; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Rocha H; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Betts M; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Schwiter R; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Butry L; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Lazzeri AL; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Frisbie LR; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Rahm AK; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Hao J; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Willard HF; Department of Population Health Sciences, Geisinger, Danville, PA, USA.
  • Martin CL; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Ledbetter DH; Genome Medical, Durham, NC, USA.
  • Williams MS; Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • Sturm AC; Autism and Developmental Medicine Institute, Geisinger, Lewisburg, PA, USA.
Genet Med ; 22(11): 1874-1882, 2020 11.
Article em En | MEDLINE | ID: mdl-32601386

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Síndrome Hereditária de Câncer de Mama e Ovário / Hiperlipoproteinemia Tipo II Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Screening_studies Limite: Female / Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Síndrome Hereditária de Câncer de Mama e Ovário / Hiperlipoproteinemia Tipo II Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Screening_studies Limite: Female / Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos