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Liu, N. et al. (n.d.). Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. Human molecular genetics. pp. 2454-2465. [Online].
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Liu, N. et al. (n.d.). Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. Human molecular genetics. pp. 2454-2465. [Online].