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Perspectives of Rare Disease Experts on Newborn Genome Sequencing.
Gold, Nina B; Adelson, Sophia M; Shah, Nidhi; Williams, Shardae; Bick, Sarah L; Zoltick, Emilie S; Gold, Jessica I; Strong, Alanna; Ganetzky, Rebecca; Roberts, Amy E; Walker, Melissa; Holtz, Alexander M; Sankaran, Vijay G; Delmonte, Ottavia; Tan, Weizhen; Holm, Ingrid A; Thiagarajah, Jay R; Kamihara, Junne; Comander, Jason; Place, Emily; Wiggs, Janey; Green, Robert C.
Afiliação
  • Gold NB; Division of Medical Genetics and Metabolism, Massachusetts General Hospital for Children, Boston.
  • Adelson SM; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
  • Shah N; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Williams S; Ariadne Labs, Boston, Massachusetts.
  • Bick SL; Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire.
  • Zoltick ES; Geisel School of Medicine, Hanover, New Hampshire.
  • Gold JI; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts.
  • Strong A; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Ganetzky R; Ariadne Labs, Boston, Massachusetts.
  • Roberts AE; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
  • Walker M; Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts.
  • Holtz AM; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Sankaran VG; Center for Healthcare Research in Pediatrics, Department of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts.
  • Delmonte O; Department of Population Medicine, Harvard Medical School, Boston, Massachusetts.
  • Tan W; Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Holm IA; Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Thiagarajah JR; Perelman School of Medicine, University of Pennsylvania, Philadelphia.
  • Kamihara J; Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Comander J; Perelman School of Medicine, University of Pennsylvania, Philadelphia.
  • Place E; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
  • Wiggs J; Department of Cardiology and Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
  • Green RC; Division of Pediatric Neurology, Massachusetts General Hospital for Children, Boston.
JAMA Netw Open ; 6(5): e2312231, 2023 05 01.
Article em En | MEDLINE | ID: mdl-37155167
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Condroitina Sulfatases / Doenças Raras Tipo de estudo: Diagnostic_studies / Guideline / Qualitative_research Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged / Newborn Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Condroitina Sulfatases / Doenças Raras Tipo de estudo: Diagnostic_studies / Guideline / Qualitative_research Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged / Newborn Idioma: En Ano de publicação: 2023 Tipo de documento: Article