Cite

Clinical findings associated with a de novo partial trisomy 10p11.22p15.3 and monosomy 7p22.3 detected by chromosomal microarray analysis.

MLA

Kohannim, Omid, et al. “Clinical Findings Associated with a de Novo Partial Trisomy 10p11.22p15.3 and Monosomy 7p22.3 Detected by Chromosomal Microarray Analysis.” Case Reports in Genetics, vol. 2011, 2011, p. 131768. EBSCOhost, https://doi.org/10.1155/2011/131768.



APA

Kohannim, O., Peredo, J., Dipple, K. M., & Quintero-Rivera, F. (2011). Clinical findings associated with a de novo partial trisomy 10p11.22p15.3 and monosomy 7p22.3 detected by chromosomal microarray analysis. Case Reports in Genetics, 2011, 131768. https://doi.org/10.1155/2011/131768



Chicago

Kohannim, Omid, Jane Peredo, Katrina M Dipple, and Fabiola Quintero-Rivera. 2011. “Clinical Findings Associated with a de Novo Partial Trisomy 10p11.22p15.3 and Monosomy 7p22.3 Detected by Chromosomal Microarray Analysis.” Case Reports in Genetics 2011: 131768. doi:10.1155/2011/131768.