Celestino-Soper, P. B., Shaw, C. A., Sanders, S. J., Li, J., Murtha, M. T., Ercan-Sencicek, A. G., . . . Beaudet, A. L. (2011). Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. Oxford University Press.
Citação norma ChicagoCelestino-Soper, Patricia B.S., et al. Use of Array CGH to Detect Exonic Copy Number Variants Throughout the Genome in Autism Families Detects a Novel Deletion in TMLHE. Oxford University Press, 2011.
Citação norma MLACelestino-Soper, Patricia B.S., et al. Use of Array CGH to Detect Exonic Copy Number Variants Throughout the Genome in Autism Families Detects a Novel Deletion in TMLHE. Oxford University Press, 2011.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.