Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hyoungseok Jeon"'
Autor:
Jong Seop Kim, Hyoungseok Jeon, Hyeran Lee, Jung Min Ko, Yonghwan Kim, Murim Choi, Gen Nishimura, Ok-Hwa Kim, Tae-Joon Cho
Publikováno v:
Human Genome Variation, Vol 8, Iss 1, Pp 1-4 (2021)
Abstract An 11-year-old Korean boy presented with short stature, hip dysplasia, radial head dislocation, carpal coalition, genu valgum, and fixed patellar dislocation and was clinically diagnosed with Steel syndrome. Scrutinizing the trio whole-exome
Externí odkaz:
https://doaj.org/article/0a4edcb96a304841b3a2b8dbf70456da
Autor:
Tae-Yong Choi, Hyoungseok Jeon, Sejin Jeong, Eum Ji Kim, Jeongseop Kim, Yun Ha Jeong, Byungsoo Kang, Murim Choi, Ja Wook Koo
SummarySocial animals compete for limited resources, resulting in a social hierarchy. Although different neuronal subpopulations in the medial prefrontal cortex (mPFC), a hub brain region of social hierarchy, encode distinct social competition behavi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::199fb36ea2808c44d8393b05f8defdd2
https://doi.org/10.1101/2023.01.04.522808
https://doi.org/10.1101/2023.01.04.522808
Autor:
Ok Hwa Kim, Gen Nishimura, Hye Ran Lee, Jong Seop Kim, Murim Choi, Jung Min Ko, Tae Joon Cho, Yonghwan Kim, Hyoungseok Jeon
Publikováno v:
Human Genome Variation, Vol 8, Iss 1, Pp 1-4 (2021)
Human Genome Variation
Human Genome Variation
An 11-year-old Korean boy presented with short stature, hip dysplasia, radial head dislocation, carpal coalition, genu valgum, and fixed patellar dislocation and was clinically diagnosed with Steel syndrome. Scrutinizing the trio whole-exome sequenci
Autor:
Moses Lee, Woo Joong Kim, Soo Yeon Kim, Murim Choi, Sangmoon Lee, Jong Hee Chae, Jin Sook Lee, H.S. Kim, Jon Soo Kim, Won Seop Kim, Jeongeun Lee, Anna Cho, Youngha Lee, Yongjin Yoo, Eun Young Jeon, Jaeso Cho, Jung Min Ko, Jieun Seo, Jana Kneissl, Soo Jin Park, Jean Lee, Hyoungseok Jeon, Eunha Kim, Sung Eun Hong, Byeong Chan Lim, Taekyeong Yoo
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Scientific Reports
Scientific Reports
BackgroundA substantial portion of Mendelian disease patients suffers from genetic variants that are inherited in a recessive manner. A precise understanding of pathogenic recessive variants in a population would assist in pre-screening births of suc
Autor:
Ja Wook Koo, Hyoungseok Jeon, Jeong Seop Kim, Murim Choi, Se Jin Jeong, Byungsoo Kang, Tae-Yong Choi, Yun Ha Jeong
Publikováno v:
IBRO Reports. 6:S186