Kumar, V., Roy, S., & Kumar, G. (2018). An Interesting and Unique Case of 8p23.3p23.1 Deletion and 8p23.1p11.1 Interstitial Duplication Syndrome. J Pediatr Genet.
Chicago-tyylinen lähdeviittausKumar, Vivek, Shuvendu Roy, ja Gaurav Kumar. "An Interesting and Unique Case of 8p23.3p23.1 Deletion and 8p23.1p11.1 Interstitial Duplication Syndrome." J Pediatr Genet 2018.
MLA-viiteKumar, Vivek, Shuvendu Roy, ja Gaurav Kumar. "An Interesting and Unique Case of 8p23.3p23.1 Deletion and 8p23.1p11.1 Interstitial Duplication Syndrome." J Pediatr Genet 2018.
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