Slavotinek, A., Risolino, M., Losa, M., Cho, M. T., Monaghan, K. G., Schneidman-Duhovny, D., . . . Shieh, J. (2017). De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects. Hum Mol Genet.
Chicago Style CitationSlavotinek, Anne, et al. "De Novo, Deleterious Sequence Variants That Alter the Transcriptional Activity of the Homeoprotein PBX1 Are Associated With Intellectual Disability and Pleiotropic Developmental Defects." Hum Mol Genet 2017.
Cita MLASlavotinek, Anne, et al. "De Novo, Deleterious Sequence Variants That Alter the Transcriptional Activity of the Homeoprotein PBX1 Are Associated With Intellectual Disability and Pleiotropic Developmental Defects." Hum Mol Genet 2017.