المؤلفون: Kim, Jong Seop, Jeon, Hyoungseok, Lee, Hyeran, Ko, Jung Min, Kim, Yonghwan, Choi, Murim, Nishimura, Gen, Kim, Ok-Hwa, Cho, Tae-Joon

المصدر: Human Genome Variation; 5/7/2021, Vol. 8 Issue 1, p1-4, 4p

مصطلحات موضوعية: GENETIC mutation, STATURE, GENU valgum, DYSPLASIA, EXOMES

المؤلفون: Kim, Boram, Kim, Man Jin, Hur, Keunyoung, Jo, Seong Jin, Ko, Jung Min, Park, Sung Sup, Seong, Moon-Woo, Mun, Je-Ho

المصدر: Scientific Reports; 1/13/2021, Vol. 11 Issue 1, p1-7, 7p

مصطلحات موضوعية: BASAL cell nevus syndrome, PHENOTYPES, GENE amplification, GENETIC testing, BASAL cell carcinoma

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: Cha, Hwa, Lee, Ok-Kyu, Kim, Soo, Ko, Jung-Min, Kim, Su, Son, Ji, Han, Hyun, Li, Shunhua, Ahn, Kyu, An, In-Sook, An, Sungkwan, Bae, Seunghee

المصدر: Molecular & Cellular Toxicology; Mar2015, Vol. 11 Issue 1, p19-28, 10p

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: Jung Min Ko, Chong-Kun Cheon, Gu-Hwan Kim, Han-Wook Yoo, Ko, Jung Min, Cheon, Chong-Kun, Kim, Gu-Hwan, Yoo, Han-Wook

المصدر: European Journal of Pediatrics; Jul2009, Vol. 168 Issue 7, p877-880, 4p, 1 Color Photograph, 1 Black and White Photograph, 1 Chart, 1 Graph

مصطلحات موضوعية: SKELETON, GENETIC mutation, GENITALIA, TENNIS elbow, ADRENOCORTICOTROPIC hormone, 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

المؤلفون: Lee, Min Jeong (AUTHOR), Park, Ji Soo¹ (AUTHOR), Kim, Kyunghoon^1,2 (AUTHOR), Ko, Jung Min (AUTHOR), Park, June Dong (AUTHOR), Suh, Dong In (AUTHOR)

المصدر: European Journal of Pediatrics. May2024, p1-9.