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 ZitierstilSlavotinek, 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.
MLA ZitierstilSlavotinek, 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.