المؤلفون: Kim, Ka Young, Heo, You Joung, Ko, Jung Min, Lee, Young Ah, Shin, Choong Ho, Ki, Chang Seok, Lee, Yun Jeong

المصدر: BMC Endocrine Disorders; 4/15/2024, Vol. 24 Issue 1, p1-6, 6p

مصطلحات موضوعية: HDL cholesterol, HYPERCHOLESTEREMIA, HYPERLIPOPROTEINEMIA, AUTOANTIBODIES, POLYMERASE chain reaction, GENE expression, PANCREATITIS, LIPASES, TRIGLYCERIDES, GENETIC mutation, ELECTROPHORESIS, GENETIC testing, SEQUENCE analysis

المؤلفون: Choi, Naye, Kim, Hwa Young, Lim, Byung Chan, Chae, Jong‐Hee, Kim, Soo Yeon, Ko, Jung Min

المصدر: Molecular Genetics & Genomic Medicine; Oct2021, Vol. 9 Issue 10, p1-16, 16p

مصطلحات موضوعية: KOREANS, THUMB, GENETIC mutation, CONGENITAL heart disease, SHORT stature, HUMAN abnormalities

مصطلحات جغرافية: SOUTH Korea

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, Hwa Young, Song, Hyun Beom, Kim, Kyu Han, Kim, Jeong Hun, Chae, Jong‐Hee, Kim, Man Jin, Seong, Moon‐Woo, Ko, Jung Min

المصدر: Experimental Dermatology; May2021, Vol. 30 Issue 5, p676-683, 8p

مصطلحات موضوعية: NF-kappa B, GENETIC mutation, GENETIC counseling, DELETION mutation, CUTANEOUS manifestations of general diseases

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: 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: Ko, Jung Min¹ jmko@snu.ac.kr, Sohn, Young Bae², Jeong, Seon Yong², Kim, Hyon-Ju², Messiaen, Ludwine M.³

المصدر: Pediatric Neurology. Jun2013, Vol. 48 Issue 6, p447-453. 7p.

مصطلحات موضوعية: *GENETIC mutation, *NEUROFIBROMATOSIS 1, *GENETIC disorders, *PSEUDOGENES, *MOLECULAR genetics, *POLYMERASE chain reaction

مصطلحات جغرافية: KOREA

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: Kim, Jae-hyung¹ (AUTHOR), Ko, Jung Min² (AUTHOR) jmko@snu.ac.kr, Tchah, Hungwon³ (AUTHOR)

المصدر: Ophthalmic Genetics. Sep2015, Vol. 36 Issue 3, p284-286. 3p.

مصطلحات موضوعية: *RETINAL degeneration, *CONGENITAL disorders, *ENDOTHELIAL cells, *GENETIC mutation, *SODIUM bicarbonate, *DNA analysis

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