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APA Citation

    Liu, N., Schoch, K., Luo, X., Pena, L. D. M., Bhavana, V. H., Kukolich, M. K., Stringer, S., Powis, Z., Radtke, K., Mroske, C., Deak, K. L., McDonald, M. T., McConkie-Rosell, A., Markert, M. L., Kranz, P. G., Stong, N., Need, A. C., Bick, D., Amaral, M. D., Worthey, E. A., Levy, S., , , Wangler, M. F., Bellen, H. J., Shashi, V., & Yamamoto, S. (n.d.). functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. Human molecular genetics, 27, 2454–2465. http://access.bl.uk/ark:/81055/vdc_100095491580.0x000026
  
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