Your browser doesn't support javascript.
loading
Response to Zhang et al.
Hart, Sarah J; Zimmerman, Kanecia; Linardic, Corinne M; Cannon, Sheila; Pastore, Anna; Patsiogiannis, Vasiliki; Rossi, Paolo; Santoro, Stephanie L; Skotko, Brian G; Torres, Amy; Valentini, Diletta; Vellody, Kishore; Worley, Gordon; Kishnani, Priya S.
Afiliación
  • Hart SJ; Department of Pediatrics, Duke University Medical Center, Durham, NC, USA. sarah.hart@duke.edu.
  • Zimmerman K; Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
  • Linardic CM; Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
  • Cannon S; Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, USA.
  • Pastore A; Down Syndrome Center of Western Pennsylvania, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
  • Patsiogiannis V; Laboratory of Molecular Genetics and Functional Genomics, Division of Genetic and Rare Disease, Bambino Gesù Children's Hospital and Research Institute, Rome, Italy.
  • Rossi P; Down Syndrome Program, Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Rome, Italy.
  • Santoro SL; Laboratory of Molecular Genetics and Functional Genomics, Division of Genetic and Rare Disease, Bambino Gesù Children's Hospital and Research Institute, Rome, Italy.
  • Skotko BG; Department of Pediatrics, Bambino Gesù Children's Hospital and Research Institute, Rome, Italy.
  • Torres A; Down Syndrome Program, Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Rome, Italy.
  • Valentini D; Division of Genetics, Nationwide Children's Hospital, Columbus, OH, USA.
  • Vellody K; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
  • Worley G; Down Syndrome Program, Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Rome, Italy.
  • Kishnani PS; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.
Genet Med ; 22(3): 662, 2020 03.
Article en En | MEDLINE | ID: mdl-31712672
Asunto(s)
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Down / Anemia Ferropénica Límite: Child / Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Down / Anemia Ferropénica Límite: Child / Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos