Publications
Filters: Author is Mo, Guiling [Clear All Filters]
A novel KMT2D mutation resulting in Kabuki syndrome: A case report." Molecular Medicine Reports. 2016.
"Notice: This site is no longer being actively maintained. While much of the information is still relevant, some of it has become out-of-date.
There are several Facebook groups. Just search "Kabuki syndrome" from within Facebook.
For a current site see one of the following:
http://allthingskabuki.org
https://www.kabukisyndromefoundation.org