Presentation
Complex Cases of KBG Syndrome Due to Mutations in ANKRD11: Blended Phenotypes, Parental Inheritance, and Potential Phenotypic Expansion to Include Hearing Loss
DW Smith Workshop
(2017)
Disciplines
Publication Date
2017
Location
Vermont
Citation Information
Maria Descartes, et al. "Complex Cases of KBG Syndrome Due to Mutations in ANKRD11: Blended Phenotypes, Parental Inheritance, and Potential Phenotypic Expansion to Include Hearing Loss" DW Smith Workshop (2017) Available at: http://works.bepress.com/maria-descartes/156/