Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease

Ivan Y Iourov, Svetlana G Vorsanova, Victoria Y Voinova, Oxana S Kurinnaia, Maria A Zelenova, Irina A Demidova, Yuri B Yurov
  • Molecular Cytogenetics, January 2013, Springer Science + Business Media
  • DOI: 10.1186/1755-8166-6-53

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The following have contributed to this page: Maria Zelenova