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Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease.
Terhune, Elizabeth A; Wethey, Cambria I; Cuevas, Melissa T; Monley, Anna M; Baschal, Erin E; Bland, Morgan R; Baschal, Robin; Trahan, G Devon; Taylor, Matthew R G; Jones, Kenneth L; Hadley Miller, Nancy.
Afiliação
  • Terhune EA; Department of Orthopedics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Wethey CI; Department of Orthopedics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Cuevas MT; Department of Orthopedics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Monley AM; Department of Orthopedics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Baschal EE; Musculoskeletal Research Center, Children's Hospital Colorado, Aurora, CO 80045, USA.
  • Bland MR; Department of Orthopedics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Baschal R; Department of Orthopedics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Trahan GD; Department of Orthopedics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Taylor MRG; Musculoskeletal Research Center, Children's Hospital Colorado, Aurora, CO 80045, USA.
  • Jones KL; Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
  • Hadley Miller N; Department of Medicine, Adult Medical Genetics Program, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Genes (Basel) ; 12(6)2021 06 16.
Article em En | MEDLINE | ID: mdl-34208743
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Escoliose / Citoesqueleto / Herança Multifatorial Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Genes (Basel) Ano de publicação: 2021 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: Polimorfismo Genético / Escoliose / Citoesqueleto / Herança Multifatorial Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Genes (Basel) Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos