المؤلفون: Lee, Yena, Choi, Yunha, Seo, Go Hun, Kim, Gu-Hwan, Choi, In Hee, Keum, Changwon, Ko, Jung Min, Cheon, Chong Kun, Jeon, Jihyun, Choi, Jin-Ho, Yoo, Han-Wook, Lee, Beom Hee

المصدر: Journal of Human Genetics; April 2021, Vol. 66 Issue: 4 p389-399, 11p

المؤلفون: Kim, Dahye, Ko, Jung Min, Kim, Yoon-myung, Seo, Go Hun, Kim, Gu-Hwan, Lee, Beom Hee, Yoo, Han-Wook

المصدر: Journal of Human Genetics; August 2018, Vol. 63 Issue: 8 p911-917, 7p

المؤلفون: Choi, Jin-Ho, Lee, Beom Hee, Kim, Ja Hye, Kim, Gu-Hwan, Kim, Yoo-Mi, Cho, Jahyang, Cheon, Chong-Kun, Ko, Jung Min, Lee, Jung Hyun, Yoo, Han-Wook

المصدر: Journal of Human Genetics; Sep2015, Vol. 60 Issue 9, p501-507, 7p

مصطلحات موضوعية: ORNITHINE carbamoyltransferase deficiency, GENETIC mutation, X-linked genetic disorders, PHENOTYPES, MOLECULAR spectroscopy, HEALTH outcome assessment

المؤلفون: Sohn, Young Bae, Ko, Jung Min, Shin, Choong Ho, Yang, Sei Won, Chae, Jong-Hee, Lee, Kyung-A

المصدر: Journal of Human Genetics; March 2016, Vol. 61 Issue: 3 p235-239, 5p

المؤلفون: Cheon, Chong Kun, Sohn, Young Bae, Ko, Jung Min, Lee, Yeoun Joo, Song, Ji Sun, Moon, Jea Woo, Yang, Bo Kyoung, Ha, Il Soo, Bae, Eun Jung, Jin, Hyun-Seok, Jeong, Seon-Yong

المصدر: Journal of Human Genetics; Jun2014, Vol. 59 Issue 6, p321-325, 5p

مصطلحات موضوعية: KABUKI syndrome, INTELLECTUAL disabilities, GENETIC mutation, NUCLEOTIDE sequence, KOREANS, GENETIC engineering, PATIENTS, DISEASES

المؤلفون: Seo, Jieun, Choi, In-Ho, Lee, Je Sang, Yoo, Yongjin, Kim, Nayoung KD, Choi, Murim, Ko, Jung Min, Shin, Yong Beom

المصدر: Journal of Human Genetics; Apr2015, Vol. 60 Issue 4, p213-215, 3p

مصطلحات موضوعية: AKABANE disease, PTERYGIUM, GENETIC mutation, CHOLINERGIC receptors, MALOCCLUSION, SCIENTIFIC observation, FRAMESHIFT mutation, ARTHROGRYPOSIS, DIAGNOSIS