Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia
Authors
Aslı Sırmacı,
Michail SpiliopoulosFrancesco Brancati,
Eric Powell,
Duygu Duman,
Alex Abrams,
Güney Bademci,
Emanuele Agolini,
Shengru Guo,
Berrin Konuk,
Aslı Kavaz,
Susan Blanton,
M. Digilio,
Bruno Dallapiccola,
Juan Young,
Stephan Züchner +14 authors
,
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