Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature

MLA

Haiyu Li, et al. “Rare Partial Octosomy and Hexasomy of 15q11-Q13 Associated with Intellectual Impairment and Development Delay: Report of Two Cases and Review of Literature.” Molecular Cytogenetics, vol. 11, no. 1, Feb. 2018, pp. 1–8. EBSCOhost, https://doi.org/10.1186/s13039-018-0365-5.

APA

Haiyu Li, Juan Du, Wen Li, Dehua Cheng, Wenbin He, Duo Yi, Bo Xiong, Shimin Yuan, Chaofeng Tu, Lanlan Meng, Aixiang Luo, Ge Lin, Guangxiu Lu, & Yue-Qiu Tan. (2018). Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature. Molecular Cytogenetics, 11(1), 1–8. https://doi.org/10.1186/s13039-018-0365-5

Chicago

Haiyu Li, Juan Du, Wen Li, Dehua Cheng, Wenbin He, Duo Yi, Bo Xiong, et al. 2018. “Rare Partial Octosomy and Hexasomy of 15q11-Q13 Associated with Intellectual Impairment and Development Delay: Report of Two Cases and Review of Literature.” Molecular Cytogenetics 11 (1): 1–8. doi:10.1186/s13039-018-0365-5.