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Development of a genomic DNA reference material panel for Rett syndrome (MECP2-related disorders) genetic testing.
Kalman, Lisa V; Tarleton, Jack C; Percy, Alan K; Aradhya, Swaroop; Bale, Sherri; Barker, Shannon D; Bayrak-Toydemir, Pinar; Bridges, Christina; Buller-Burckle, Arlene M; Das, Soma; Iyer, Ramaswamy K; Vo, Timothy D; Zvereff, Val V; Toji, Lorraine H.
Afiliación
  • Kalman LV; Laboratory Research and Evaluation Branch, Centers for Disease Control and Prevention, Atlanta, Georgia. Electronic address: lkalman@cdc.gov.
  • Tarleton JC; Fullerton Genetics Laboratory, Fullerton Genetics Center, Mission Health System, Asheville, North Carolina.
  • Percy AK; Intellectual and Developmental Disabilities Research Center, University of Alabama, Birmingham, Birmingham, Alabama.
  • Aradhya S; Neurogenetics, GeneDx, Gaithersburg, Maryland.
  • Bale S; Neurogenetics, GeneDx, Gaithersburg, Maryland.
  • Barker SD; Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia.
  • Bayrak-Toydemir P; Molecular Genetics and Genomics Laboratory, ARUP Laboratories, Salt Lake City, Utah.
  • Bridges C; Fullerton Genetics Laboratory, Fullerton Genetics Center, Mission Health System, Asheville, North Carolina.
  • Buller-Burckle AM; Molecular Genetics, Quest Diagnostics Nichols Institute, San Juan Capistrano, California.
  • Das S; Department of Human Genetics, University of Chicago, Chicago, Illinois.
  • Iyer RK; Molecular Genetics Laboratory, Michigan Medical Genetics Laboratories, University of Michigan Medical Center, Ann Arbor, Michigan.
  • Vo TD; Ambry Genetics, Aliso Viejo, California.
  • Zvereff VV; Molecular Genetics & Genomics, Laboratory Corporation of America, Research Triangle Park, North Carolina.
  • Toji LH; NIGMS Human Genetic Cell Repository, Coriell Institute for Medical Research, Camden, New Jersey.
J Mol Diagn ; 16(2): 273-9, 2014 Mar.
Article en En | MEDLINE | ID: mdl-24508304
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estándares de Referencia / Síndrome de Rett / Pruebas Genéticas / Proteína 2 de Unión a Metil-CpG Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: J Mol Diagn Asunto de la revista: BIOLOGIA MOLECULAR Año: 2014 Tipo del documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estándares de Referencia / Síndrome de Rett / Pruebas Genéticas / Proteína 2 de Unión a Metil-CpG Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: J Mol Diagn Asunto de la revista: BIOLOGIA MOLECULAR Año: 2014 Tipo del documento: Article