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.
Dyfyniad Arddull ChicagoIourov, 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.
Dyfyniad MLAIourov, 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.