Citace podle APA

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.

Styl Chicago

Dinwiddie, Darrell L., Sarah E. Soden, Carol J. Saunders, Neil A. Miller, Emily G. Farrow, Laurie D. Smith, a Stephen F. Kingsmore. De Novo Frameshift Mutation in ASXL3 in a Patient With Global Developmental Delay, Microcephaly, and Craniofacial Anomalies. BioMed Central, 2013.

Citace podle MLA

Dinwiddie, Darrell L., et al. De Novo Frameshift Mutation in ASXL3 in a Patient With Global Developmental Delay, Microcephaly, and Craniofacial Anomalies. BioMed Central, 2013.

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