Hyung-Goo Kim
Work Details:
Department: OB/GYN
Institution: Georgia Regents University
Course: Institute of Molecular Medicine and Genetics
Institution (in Local Language):
Research:
Article Title/DOI: Disruption of neurexin 1 associated with autism spectrum disorder
Journal: American Journal of Human Genetics
VOL: 2008
Article Title: Mutations in CHD7 encoding a chromatin-remodeling protein cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
Journal: American Journal of Human Genetics
VOL: 2008
Article Title: WDR11 a WD protein that interacts with transcription factor EMX1 is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
Journal: American Journal of Human Genetics
VOL: 2010
Article Title: Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies
Journal: American Journal of Human Genetics
VOL: 2012
Article Title: Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries
Journal: Cell
VOL: 2012