Complex Cases of KBG Syndrome Due to Mutations in ANKRD11: Blended Phenotypes, Parental Inheritance, and Potential Phenotypic Expansion to Include Hearing Loss

Maria Descartes, et al; Maria Descartes

Complex Cases of KBG Syndrome Due to Mutations in ANKRD11: Blended Phenotypes, Parental Inheritance, and Potential Phenotypic Expansion to Include Hearing Loss

Maria Descartes, et al, Maria Descartes

Research output: Contribution to conference › Presentation

Original language	American English
State	Published - 2017
Event	DW Smith Workshop - Vermont Duration: Jan 1 2017 → …

Conference

Conference	DW Smith Workshop
Period	1/1/17 → …

Disciplines

Medicine and Health Sciences

Cite this

@conference{32cea62c90924cfc86728428597e7cbe,

title = "Complex Cases of KBG Syndrome Due to Mutations in ANKRD11: Blended Phenotypes, Parental Inheritance, and Potential Phenotypic Expansion to Include Hearing Loss",

author = "{Descartes, et al}, Maria and Maria Descartes",

year = "2017",

language = "American English",

note = "DW Smith Workshop ; Conference date: 01-01-2017",

}