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FISH ( Fluorescence in situ hybridization ) 을 이용한 신속한 산전 염색체 이수성 ( Aneuploidies ) 진단

DC FieldValueLanguage
dc.contributor.author김인규-
dc.date.accessioned2020-07-02T17:28:39Z-
dc.date.available2020-07-02T17:28:39Z-
dc.date.issued1998-
dc.identifier.issn0494-4755-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/176834-
dc.description.abstractIntroduction: The traditional cytogenetic analysis requires relatively long cell culture time, intensive labour and trained personnel. But in clinical situations, the prenatal diagnosis of genetic disease and incidental finding of abnormal ultrasonographic finding need urgent decisions on future management. So we need more rapid and precise diagnostic tools of prenatal genetic counselling. The fluorescence in situ hybridization (FISH) has been studied for detecting chromosomal aneuploidies because this method can get rapid results of cytogenetic studies. Objectives: To evaluate the clinical utility of prenatal diagnosis of chromosomal aneuploidies by using FISH. Materials and methods: chorionic villi (n=6), amniotic fluid (n=7), fetal blood (n=2) were obtained from 15 pregnancies undergoing fetal karyotyping at 9 to 30 weeks of gestation for prenatal genetic counselling.Karyotyping was performed by both traditional cytogenetics and FISH, using commertially available kits. After the procedures, the results of FISH were compared with the results of traditional cytogenetic studies. Results: In a blind series of 15 samples all, including one case of trisomy 21, one case of trisomy 18 and one case of monosomy X, were correctly identified. Conclusions: FISH is a rapid and effective methods for detection of chromosomal aneuploidies in prenatal diagnosis and yields possible clue of fetal genetic diagnosis with pregnant maternal peripheral blood.-
dc.description.statementOfResponsibilityrestriction-
dc.languageKorean-
dc.publisher대한산부인과학회-
dc.relation.isPartOfKorean Journal of Obstetrics and Gynecology (대한산부인과학회잡지)-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleFISH ( Fluorescence in situ hybridization ) 을 이용한 신속한 산전 염색체 이수성 ( Aneuploidies ) 진단-
dc.title.alternativeRapid Prenatal Diagnosis of Chromosomal Aneuploidies by Using Fluorescence in Situ Hybridization ( FISH )-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Obstetrics and Gynecology (산부인과학교실)-
dc.contributor.googleauthor김인규-
dc.contributor.googleauthor양영호-
dc.contributor.googleauthor최은경-
dc.contributor.googleauthor김미순-
dc.contributor.googleauthor김진영-
dc.contributor.localIdA00839-
dc.relation.journalcodeJ02075-
dc.identifier.urlhttp://kiss.kstudy.com/journal/thesis_name.asp?tname=kiss2002&key=1856747-
dc.contributor.alternativeNameKim, In Kyu-
dc.contributor.affiliatedAuthor김인규-
dc.citation.volume41-
dc.citation.number5-
dc.citation.startPage1315-
dc.citation.endPage1322-
dc.identifier.bibliographicCitationKorean Journal of Obstetrics and Gynecology (대한산부인과학회잡지), Vol.41(5) : 1315-1322, 1998-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers

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