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. BioMed Central.
Chicago Style CitationIourov, 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. BioMed Central, 2015.
MLA CitationIourov, 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. BioMed Central, 2015.