Your browser doesn't support javascript.
loading
Phenotypic expansion and variable expressivity in individuals with JARID2-related intellectual disability: A case series.
Cadieux-Dion, Maxime; Farrow, Emily; Thiffault, Isabelle; Cohen, Ana S A; Welsh, Holly; Bartik, Lauren; Schwager, Caitlin; Engleman, Kendra; Zhou, Dihong; Zhang, Lei; Repnikova, Elena; Amudhavalli, Shivarajan M; Saunders, Carol J.
Afiliação
  • Cadieux-Dion M; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA.
  • Farrow E; Department of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, USA.
  • Thiffault I; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA.
  • Cohen ASA; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA.
  • Welsh H; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA.
  • Bartik L; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA.
  • Schwager C; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA.
  • Engleman K; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, Missouri, USA.
  • Zhou D; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA.
  • Zhang L; Genomic Medicine Center, Children's Mercy Hospital, Kansas City, Missouri, USA.
  • Repnikova E; Department of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, USA.
  • Amudhavalli SM; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA.
  • Saunders CJ; Department of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, USA.
Clin Genet ; 102(2): 136-141, 2022 08.
Article em En | MEDLINE | ID: mdl-35533077
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Autístico / Deficiência Intelectual Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Clin Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Autístico / Deficiência Intelectual Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Clin Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos