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Human genetics and molecular genomics of Chiari malformation type 1.
Mekbib, Kedous Y; Muñoz, William; Allington, Garrett; McGee, Stephen; Mehta, Neel H; Shofi, John P; Fortes, Carla; Le, Hao Thi; Nelson-Williams, Carol; Nanda, Pranav; Dennis, Evan; Kundishora, Adam J; Khanna, Arjun; Smith, Hannah; Ocken, Jack; Greenberg, Ana B W; Wu, Rui; Moreno-De-Luca, Andres; DeSpenza, Tyrone; Zhao, Shujuan; Marlier, Arnaud; Jin, Sheng Chih; Alper, Seth L; Butler, William E; Kahle, Kristopher T.
Afiliación
  • Mekbib KY; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA; Harvard Center for Hydrocephalus and Neurodevelopmental Disorders, Massachusetts General Hospital, Boston, MA, USA.
  • Muñoz W; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA; Harvard Center for Hydrocephalus and Neurodevelopmental Disorders, Massachusetts General Hospital, Boston, MA, USA.
  • Allington G; Department of Pathology, Yale University School of Medicine, New Haven, CT, USA.
  • McGee S; GeneDx, Gaithersburg, MD, USA.
  • Mehta NH; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Shofi JP; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Fortes C; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Le HT; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Nelson-Williams C; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • Nanda P; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Dennis E; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Kundishora AJ; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA.
  • Khanna A; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Smith H; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Ocken J; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA.
  • Greenberg ABW; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Wu R; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Moreno-De-Luca A; Department of Radiology, Autism and Developmental Medicine Institute, Genomic Medicine Institute, Geisinger, Danville, PA, USA.
  • DeSpenza T; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA.
  • Zhao S; Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA.
  • Marlier A; Altos Labs, San Diego, CA, USA.
  • Jin SC; Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA; Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA.
  • Alper SL; Division of Nephrology and Vascular Biology Research Center, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA; Department of Medicine, Harvard Medical School, Boston, MA, USA.
  • Butler WE; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
  • Kahle KT; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA; Harvard Center for Hydrocephalus and Neurodevelopmental Disorders, Massachusetts General Hospital, Boston, MA, USA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA; Broad Institute of MIT and
Trends Mol Med ; 29(12): 1059-1075, 2023 12.
Article en En | MEDLINE | ID: mdl-37802664
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Malformación de Arnold-Chiari / Encefalopatías Límite: Humans Idioma: En Revista: Trends Mol Med Asunto de la revista: BIOLOGIA MOLECULAR Año: 2023 Tipo del documento: Article País de afiliación: 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: Malformación de Arnold-Chiari / Encefalopatías Límite: Humans Idioma: En Revista: Trends Mol Med Asunto de la revista: BIOLOGIA MOLECULAR Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos