Iourov, I. Y., Vorsanova, S. G., Voinova, V. Y., Kurinnaia, O. S., Zelenova, M. A., Demidova, I. A., & Yurov, Y. B. (2013). Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease. BioMed Central.

Iourov, Ivan Y., Svetlana G. Vorsanova, Victoria Y. Voinova, Oxana S. Kurinnaia, Maria A. Zelenova, Irina A. Demidova, and Yuri B. Yurov. Xq28 (MECP2) Microdeletions Are Common in Mutation-negative Females With Rett Syndrome and Cause Mild Subtypes of the Disease. BioMed Central, 2013.

Iourov, Ivan Y., et al. Xq28 (MECP2) Microdeletions Are Common in Mutation-negative Females With Rett Syndrome and Cause Mild Subtypes of the Disease. BioMed Central, 2013.