Wen, J., Lopes, F., Soares, G., Farrell, S. A., Nelson, C., Qiao, Y., . . . Rajcan-Separovic, E. (2013). Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2. Orphanet Journal of Rare Diseases, 8(1), 100-101.
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Cita Chicago Style (17a ed.)
Wen, Jiadi, et al. "Phenotypic and Functional Consequences of Haploinsufficiency of Genes from Exocyst and Retinoic Acid Pathway Due to a Recurrent Microdeletion of 2p13.2."
Orphanet Journal of Rare Diseases 8, no. 1 (2013): 100-101.
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Cita MLA (9a ed.)
Wen, Jiadi, et al. "Phenotypic and Functional Consequences of Haploinsufficiency of Genes from Exocyst and Retinoic Acid Pathway Due to a Recurrent Microdeletion of 2p13.2."
Orphanet Journal of Rare Diseases, vol. 8, no. 1, 2013, pp. 100-101.
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