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.
シカゴスタイル引用形Iourov, Ivan Y., Svetlana G. Vorsanova, Victoria Y. Voinova, Oxana S. Kurinnaia, Maria A. Zelenova, Irina A. Demidova, , 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.
MLA引用形式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.