Vol 34: A de novo Microdeletion of ANKRD11 Gene in a Korean Patient with KBG Syndrome.Report as inadecuate



 Vol 34: A de novo Microdeletion of ANKRD11 Gene in a Korean Patient with KBG Syndrome.


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This article is from Annals of Laboratory Medicine, volume 34.AbstractKBG syndrome is a very rare genetic disorder characterized by macrodontia of upper central incisors, global developmental delay, distinctive craniofacial features, short stature, and skeletal anomalies. Ankyrin repeat domain 11 gene (ANKRD11) has recently been identified as a cau

Author: Lim, Ji-Hun; Seo, Eul-Ju; Kim, Yoo-Mi; Cho, Hyun-Ju; Lee, Jin-Ok; Cheon, Chong Kun; Yoo, Han-Wook

Source: https://archive.org/







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