Compound heterozygous microdeletion of chromosome 15q13.3 region in a child with hypotonia, impaired vision, and global developmental delay.

MLA

Prasun, Pankaj, et al. “Compound Heterozygous Microdeletion of Chromosome 15q13.3 Region in a Child with Hypotonia, Impaired Vision, and Global Developmental Delay.” American Journal of Medical Genetics. Part A, vol. 164A, no. 7, July 2014, pp. 1815–20. EBSCOhost, https://doi.org/10.1002/ajmg.a.36535.

APA

Prasun, P., Hankerd, M., Kristofice, M., Scussel, L., Sivaswamy, L., & Ebrahim, S. (2014). Compound heterozygous microdeletion of chromosome 15q13.3 region in a child with hypotonia, impaired vision, and global developmental delay. American Journal of Medical Genetics. Part A, 164A(7), 1815–1820. https://doi.org/10.1002/ajmg.a.36535

Chicago

Prasun, Pankaj, Michael Hankerd, Melissa Kristofice, Lindsey Scussel, Lalitha Sivaswamy, and Salah Ebrahim. 2014. “Compound Heterozygous Microdeletion of Chromosome 15q13.3 Region in a Child with Hypotonia, Impaired Vision, and Global Developmental Delay.” American Journal of Medical Genetics. Part A 164A (7): 1815–20. doi:10.1002/ajmg.a.36535.