Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Hyon Ju Kim"'
Publikováno v:
The Korean Journal of Japanese Education. 59:105-117
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02878e7e83489b063524961731519285
https://doi.org/10.21808/kjje.59.07
https://doi.org/10.21808/kjje.59.07
Autor:
Eriko Kudo, Hyon-ju Kim
Publikováno v:
The Korean Journal of Japanese Education. 40:27-43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f28e478a091ef8cbbefb621143f7cd5a
https://doi.org/10.21808/kjje.40.03
https://doi.org/10.21808/kjje.40.03
Publikováno v:
Journal of Genetic Medicine. 7:145-150
Acrodysostosis is an extremely rare disorder characterized by short fingers and toes with peripheral dysostosis, nasal hypoplasia, and mental retardation. We report a 16-year-old Korean boy with acro- dysostosis who had characteristic clinical featur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8043d5831f452e797af8e3c1a7c14db3
https://doi.org/10.5734/jgm.2010.7.2.145
https://doi.org/10.5734/jgm.2010.7.2.145
Publikováno v:
Journal of Genetic Medicine. 7:37-44
Purpose : Kabuki syndrome is a multiple congenital malformation syndrome with mental retardation. It was named after its characteristic appearance, a face resembling that of an actor in a Kabuki play. To date, six Korean cases of Kabuki syndrome have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4f1da09de3594de959baf2d98462841
https://doi.org/10.5734/jgm.2010.7.1.37
https://doi.org/10.5734/jgm.2010.7.1.37
Autor:
Hyon-Ju Kim, Kumiko Kaneniwa
Publikováno v:
The Japanese Language Association Of Korea. 50:3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ab0b456485d99116508e445a11a974c
https://doi.org/10.14817/jlak.2016.12.50.03
https://doi.org/10.14817/jlak.2016.12.50.03
Publikováno v:
Yonsei medical journal. 41(3)
To determine the precise chromosomal localization of tyrosine related protein-1 and -2 (TRP-1 and TRP-2) genes by fluorescence in situ hybridization, we used DNAs isolated from human bacterial artificial chromosome clones. They contain genomic sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::648a0af369f66eb639504cbdbd2b56e7
https://pubmed.ncbi.nlm.nih.gov/10957896
https://pubmed.ncbi.nlm.nih.gov/10957896
Autor:
Kap Soon Ju, Sook Hwan Lee, Young Ho Yang, Je Ho Lee, Yul Hee Cho, Jeong Hee Chun, Yong Seok Sohn, Jong In Kim, Ook Hwan Choi, Seung Bo Kim, Hyon Ju Kim
Publikováno v:
Yonsei medical journal. 40(5)
Since amniocentesis made prenatal diagnosis feasible in 1967, the method has been remarkably instrumental in obstetrical practice. A recent study conducted between 1980 and 1997 collected 11,000 amniocentesis procedures done at 10 university hospital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd8d410c93a66667ed3e62807fee5468
https://pubmed.ncbi.nlm.nih.gov/10565257
https://pubmed.ncbi.nlm.nih.gov/10565257
Publikováno v:
Clinical nuclear medicine. 24(3)
Hepatomegaly is a common manifestation in Gaucher disease. In some patients with the disease, hepatic fibrosis and portal hypertension are observed. A patient with Gaucher disease with the hepatopulmonary syndrome associated with severe cyanosis and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92a972e9a18baf4ff9ec1a2b43973dd4
https://pubmed.ncbi.nlm.nih.gov/10069725
https://pubmed.ncbi.nlm.nih.gov/10069725
Publikováno v:
Korean Journal of Physical Anthropology. 13:31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::612353c906d48f2c1aba4970fff9fa90
https://doi.org/10.11637/kjpa.2000.13.1.31
https://doi.org/10.11637/kjpa.2000.13.1.31
Autor:
Cha Gon Lee, Sang-Jin Park, Jun-No Yun, Jung Min Ko, Hyon-Ju Kim, Shin-Young Yim, Young Bae Sohn
Publikováno v:
Yonsei Medical Journal; Nov2013, Vol. 54 Issue 6, p1463-1470, 8p