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Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array.
Schenkel, Laila C; Schwartz, Charles; Skinner, Cindy; Rodenhiser, David I; Ainsworth, Peter J; Pare, Guillaume; Sadikovic, Bekim.
  • Schenkel LC; Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada.
  • Schwartz C; Center for Molecular Studies, J.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina.
  • Skinner C; Center for Molecular Studies, J.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina.
  • Rodenhiser DI; Department of Biochemistry, Oncology and Paediatrics, Western University, London, Ontario, Canada; London Regional Cancer Program, London Health Sciences Center, London, Ontario, Canada; Children's Health Research Institute, London Health Sciences Center, London, Ontario, Canada.
  • Ainsworth PJ; Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada; Department of Biochemistry, Oncology and Paediatrics, Western University, London, Ontario, Canada; London Regional Cancer Program, London Health Sciences Center, London, Ontario, Canada; Children's Health R
  • Pare G; Departments of Pathology and Molecular Medicine and Clinical Epidemiology and Biostatistics, McMaster University, Hamilton, Ontario, Canada.
  • Sadikovic B; Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada; London Regional Cancer Program, London Health Sciences Center, London, Ontario, Canada; Children's Health Research Institute, London Health Sciences Center, London, Ontario, Canada; Molecular Genetics Labor
J Mol Diagn ; 18(6): 834-841, 2016 11.
Article en En | MEDLINE | ID: mdl-27585064
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Metilación de ADN / Análisis de Secuencia por Matrices de Oligonucleótidos / Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Female / Humans / Male Idioma: En Año: 2016 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Metilación de ADN / Análisis de Secuencia por Matrices de Oligonucleótidos / Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Female / Humans / Male Idioma: En Año: 2016 Tipo del documento: Article