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Analysis of X-inactivation status in a Rett syndrome natural history study cohort.
Fang, Xiaolan; Butler, Kameryn M; Abidi, Fatima; Gass, Jennifer; Beisang, Arthur; Feyma, Timothy; Ryther, Robin C; Standridge, Shannon; Heydemann, Peter; Jones, Mary; Haas, Richard; Lieberman, David N; Marsh, Eric D; Benke, Tim A; Skinner, Steve; Neul, Jeffrey L; Percy, Alan K; Friez, Michael J; Caylor, Raymond C.
Afiliação
  • Fang X; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Butler KM; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Abidi F; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Gass J; Florida Cancer Specialists & Research Institute, Fort Myers, FL, USA.
  • Beisang A; Gillette Children's Specialty Healthcare, St. Paul, Minnesota, USA.
  • Feyma T; Gillette Children's Specialty Healthcare, St. Paul, Minnesota, USA.
  • Ryther RC; Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Standridge S; Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Heydemann P; Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
  • Jones M; Rush University Medical Center, Chicago, Illinois, USA.
  • Haas R; Oakland Children's Hospital, UCSF, Oakland, California, USA.
  • Lieberman DN; University of California San Diego, San Diego, California, USA.
  • Marsh ED; Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Benke TA; Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Skinner S; University of Colorado School of Medicine, Children's Hospital Colorado-Aurora, Denver, Colorado, USA.
  • Neul JL; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Percy AK; Vanderbilt Kennedy Center, Vanderbilt University Medical Center, Nashville TN.
  • Friez MJ; The University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Caylor RC; Greenwood Genetic Center, Greenwood, South Carolina, USA.
Mol Genet Genomic Med ; 10(5): e1917, 2022 05.
Article em En | MEDLINE | ID: mdl-35318820
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Rett Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Rett Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article