Publications

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2016

D. Wang, Ren, G. F., Zhang, H. Z., Yi, C. Y., and Peng, Z. J., “A de novo 2q35-q36.1 deletion incorporating IHH in a Chinese boy (47,XYY) with syndactyly, type III Waardenburg syndrome, and congenital heart disease.”, Genet Mol Res, vol. 15, no. 4, 2016.