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Multiomics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and noncanonical Wnt signaling dysregulation.
Lin, Isabella; Wei, Angela; Awamleh, Zain; Singh, Meghna; Ning, Aileen; Herrera, Analeyla; Russell, Bianca E; Weksberg, Rosanna; Arboleda, Valerie A.
Afiliação
  • Lin I; Department of Human Genetics.
  • Wei A; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
  • Awamleh Z; Department of Computational Medicine, UCLA, Los Angeles, California, USA.
  • Singh M; Department of Human Genetics.
  • Ning A; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
  • Herrera A; Department of Computational Medicine, UCLA, Los Angeles, California, USA.
  • Russell BE; Department of Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Weksberg R; Department of Human Genetics.
  • Arboleda VA; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
JCI Insight ; 8(10)2023 05 22.
Article em En | MEDLINE | ID: mdl-37053013
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Renais / Deficiência Intelectual Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Renais / Deficiência Intelectual Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article