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Characterization of X chromosome inactivation using integrated analysis of whole-exome and mRNA sequencing.
Szelinger, Szabolcs; Malenica, Ivana; Corneveaux, Jason J; Siniard, Ashley L; Kurdoglu, Ahmet A; Ramsey, Keri M; Schrauwen, Isabelle; Trent, Jeffrey M; Narayanan, Vinodh; Huentelman, Matthew J; Craig, David W.
Afiliación
  • Szelinger S; Center for Rare Childhood Disorders, The Translational Genomics Research Institute, Phoenix, Arizona, United States of America; Molecular and Cellular Biology Interdisciplinary Graduate Program, College of Liberal Arts and Sciences, Arizona State University, Tempe, Arizona, United States of America.
  • Malenica I; Center for Rare Childhood Disorders, The Translational Genomics Research Institute, Phoenix, Arizona, United States of America.
  • Corneveaux JJ; Center for Rare Childhood Disorders, The Translational Genomics Research Institute, Phoenix, Arizona, United States of America.
  • Siniard AL; Center for Rare Childhood Disorders, The Translational Genomics Research Institute, Phoenix, Arizona, United States of America.
  • Kurdoglu AA; Center for Rare Childhood Disorders, The Translational Genomics Research Institute, Phoenix, Arizona, United States of America.
  • Ramsey KM; Center for Rare Childhood Disorders, The Translational Genomics Research Institute, Phoenix, Arizona, United States of America.
  • Schrauwen I; Center for Rare Childhood Disorders, The Translational Genomics Research Institute, Phoenix, Arizona, United States of America; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
  • Trent JM; Genetic Basis of Human Disease Division, The Translational Genomics Research Institute, Phoenix, Arizona, United States of America.
  • Narayanan V; Center for Rare Childhood Disorders, The Translational Genomics Research Institute, Phoenix, Arizona, United States of America; Neurology Research, Barrow Neurological Institute, Phoenix, Arizona, United States of America.
  • Huentelman MJ; Center for Rare Childhood Disorders, The Translational Genomics Research Institute, Phoenix, Arizona, United States of America.
  • Craig DW; Center for Rare Childhood Disorders, The Translational Genomics Research Institute, Phoenix, Arizona, United States of America.
PLoS One ; 9(12): e113036, 2014.
Article en En | MEDLINE | ID: mdl-25503791
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ARN Mensajero / Análisis de Secuencia de ARN / Cromosomas Humanos X / Inactivación del Cromosoma X / Secuenciación de Nucleótidos de Alto Rendimiento / Enfermedades del Sistema Nervioso Límite: Adolescent / Adult / Child / Female / Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ARN Mensajero / Análisis de Secuencia de ARN / Cromosomas Humanos X / Inactivación del Cromosoma X / Secuenciación de Nucleótidos de Alto Rendimiento / Enfermedades del Sistema Nervioso Límite: Adolescent / Adult / Child / Female / Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos