Cite
Ha K, Shen Y, Graves T, et al. The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability. Mol Cytogenet. 2016;9:74doi: 10.1186/s13039-016-0286-0.
Ha, K., Shen, Y., Graves, T., Kim, C. H., & Kim, H. G. (2016). The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability. Molecular cytogenetics, 974. https://doi.org/10.1186/s13039-016-0286-0
Ha, Kyungsoo, et al. "The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability." Molecular cytogenetics vol. 9 (2016): 74. doi: https://doi.org/10.1186/s13039-016-0286-0
Ha K, Shen Y, Graves T, Kim CH, Kim HG. The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability. Mol Cytogenet. 2016 Sep 29;9:74. doi: 10.1186/s13039-016-0286-0. eCollection 2016. PMID: 27708714; PMCID: PMC5041540.
Copy
Download .nbib