Syndactyly

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.

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.