 |
|
Identification of a novel mutation in the
Yeonkyung Kim (Kim Y), Ho-Seok Lee (Lee HS), Jung-Seok Yu (Yu JS), Kangmo Ahn (Ahn K), Chang-Seok Ki (Ki CS), Jihyun Kim (Kim J)
Clin Exp Pediatr. 2014;57(1):46-49. Published online 2014 Jan 31 DOI: https://doi.org/10.3345/kjp.2014.57.1.46
|
|
Citations to this article as recorded by
 Suprameatal Cochlear Implantation in a CHARGE Patient With a Novel CHD7 Variant and KALLMANN Syndrome Phenotype: A Case Report
Akira Ganaha, Tetsuya Tono, Tadashi Kaname, Kumiko Yanagi, Teruyuki Higa, Shunsuke Kondo, Hiroyuki Maeda, Mikio Suzuki
Otology & Neurotology.2017; 38(7): 990. CrossRef Cerebellar vermis hypoplasia in CHARGE syndrome: clinical and molecular characterization of 18 unrelated Korean patients
Young Bae Sohn, Jung Min Ko, Choong Ho Shin, Sei Won Yang, Jong-Hee Chae, Kyung-A Lee
Journal of Human Genetics.2016; 61(3): 235. CrossRef Non-Homologous End Joining Repair Mechanism-Mediated Deletion of CHD7 Gene in a Patient with Typical CHARGE Syndrome
Seung Jun Lee, Jong Hee Chae, Jung Ae Lee, Sung Im Cho, Soo Hyun Seo, Hyunwoong Park, Moon-Woo Seong, Sung Sup Park
Annals of Laboratory Medicine.2015; 35(1): 141. CrossRef
|