APA引用形式

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.

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