Your browser doesn't support javascript.
loading
DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes.
Awamleh, Zain; Chater-Diehl, Eric; Choufani, Sanaa; Wei, Elizabeth; Kianmahd, Rebecca R; Yu, Anna; Chad, Lauren; Costain, Gregory; Tan, Wen-Hann; Scherer, Stephen W; Arboleda, Valerie A; Russell, Bianca E; Weksberg, Rosanna.
Afiliación
  • Awamleh Z; Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.
  • Chater-Diehl E; Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.
  • Choufani S; Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.
  • Wei E; Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.
  • Kianmahd RR; Department of Pediatrics, Division of Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
  • Yu A; Department of Pediatrics, Division of Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
  • Chad L; Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, Toronto, ON, Canada.
  • Costain G; Department of Paediatrics, University of Toronto, Toronto, ON, Canada.
  • Tan WH; Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.
  • Scherer SW; Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, Toronto, ON, Canada.
  • Arboleda VA; Department of Molecular Genetics, University of Toronto, Ontario, ON, Canada.
  • Russell BE; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA.
  • Weksberg R; Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.
Eur J Hum Genet ; 30(6): 695-702, 2022 06.
Article en En | MEDLINE | ID: mdl-35361921
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: Craneosinostosis / Discapacidad Intelectual Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido
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: Craneosinostosis / Discapacidad Intelectual Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Reino Unido