Zhao, Y., Diacou, A., Johnston, H. R., Musfee, F. I., McDonald-McGinn, D. M., McGinn, D., . . . Morrow, B. E. (2020). Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects. Am J Hum Genet.
Citação norma ChicagoZhao, Yingjie, et al. "Complete Sequence of the 22q11.2 Allele in 1,053 Subjects With 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects." Am J Hum Genet 2020.
Citação norma MLAZhao, Yingjie, et al. "Complete Sequence of the 22q11.2 Allele in 1,053 Subjects With 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects." Am J Hum Genet 2020.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.