ANKRD11

Publications

Ockeloen CW, et al. Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations. Eur J Hum Genet. 2015;23(9):1176-1185.

Goldenberg A, et al. Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation of ANKRD11. Am J Med Genet A. 2016;170(11):2847-2859.

Low K, et al. Clinical and genetic aspects of KBG syndrome. Am J Med Genet A. 2016;170(11):2835-2846.

Walz K, et al. Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome. Hum Genet. 2015;134(2):181-190.