Iourov, I. Y., Vorsanova, S. G., Voinova, V. Y., & Yurov, Y. B. (2015). 3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances. Mol Cytogenet.
Citação norma ChicagoIourov, Ivan Y., Svetlana G. Vorsanova, Victoria Y. Voinova, and Yuri B. Yurov. "3p22.1p21.31 Microdeletion Identifies CCK As Asperger Syndrome Candidate Gene and Shows the Way for Therapeutic Strategies in Chromosome Imbalances." Mol Cytogenet 2015.
Citação norma MLAIourov, Ivan Y., Svetlana G. Vorsanova, Victoria Y. Voinova, and Yuri B. Yurov. "3p22.1p21.31 Microdeletion Identifies CCK As Asperger Syndrome Candidate Gene and Shows the Way for Therapeutic Strategies in Chromosome Imbalances." Mol Cytogenet 2015.