Dinwiddie, D. L., Soden, S. E., Saunders, C. J., Miller, N. A., Farrow, E. G., Smith, L. D., & Kingsmore, S. F. (2013). De novo frameshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies. BioMed Central.
Citação norma ChicagoDinwiddie, Darrell L., Sarah E. Soden, Carol J. Saunders, Neil A. Miller, Emily G. Farrow, Laurie D. Smith, and Stephen F. Kingsmore. De Novo Frameshift Mutation in ASXL3 in a Patient With Global Developmental Delay, Microcephaly, and Craniofacial Anomalies. BioMed Central, 2013.
Citação norma MLADinwiddie, Darrell L., et al. De Novo Frameshift Mutation in ASXL3 in a Patient With Global Developmental Delay, Microcephaly, and Craniofacial Anomalies. BioMed Central, 2013.