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A Case with Balanced Chromosome Rearrangement Involving Chromosomes 9, 14, and 13 in a Woman with Recurrent Abortion

DC Field Value Language
dc.contributor.author김세광-
dc.contributor.author배상욱-
dc.date.accessioned2016-02-19T11:01:01Z-
dc.date.available2016-02-19T11:01:01Z-
dc.date.issued2001-
dc.identifier.issn0513-5796-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/142206-
dc.description.abstractA phenotypically normal couple was referred for cytogenetic evaluation due to three consecutive first-trimester spontaneous abortions. Chromosomal analysis from peripheral blood was performed according to standard cytogenetic methods using G-banding technique. The husband's karyotype was normal. The wife's karyotype showed a balanced complex chromosome rearrangement (CCR) involving chromosomes 9,14, and 13. There were three breakpoints: 9p21.2, 14q21, and 13q12.2. The karyotype was designated as 46, XX, t (9;14;13)(p21.2;q21; q12.2). Fluorescence in situ hybridization (FISH) analysis with chromosome-specific libraries of chromosomes 9,14, and 13 was performed to confirm this rare chromosome rearrangement. The result of FISH coincided with that obtained by standard cytogenetic techniques.-
dc.description.statementOfResponsibilityopen-
dc.format.extent345~348-
dc.relation.isPartOfYONSEI MEDICAL JOURNAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAbortion, Habitual/genetics*-
dc.subject.MESHAdult-
dc.subject.MESHChromosome Aberrations*-
dc.subject.MESHChromosomes, Human, Pair 13*-
dc.subject.MESHChromosomes, Human, Pair 14*-
dc.subject.MESHChromosomes, Human, Pair 9*-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHIn Situ Hybridization, Fluorescence-
dc.subject.MESHPregnancy-
dc.titleA Case with Balanced Chromosome Rearrangement Involving Chromosomes 9, 14, and 13 in a Woman with Recurrent Abortion-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Obstetrics & Gynecology (산부인과학)-
dc.contributor.googleauthorSei Kwang Kim-
dc.contributor.googleauthorHyon Ju Kim-
dc.contributor.googleauthorYoung Ho Yang-
dc.contributor.googleauthorIn Kyu Kim-
dc.contributor.googleauthorSang Wook Bai-
dc.contributor.googleauthorJeong Yeon Kim-
dc.contributor.googleauthorKi Hyun Park-
dc.contributor.googleauthorDong Jae Cho-
dc.contributor.googleauthorChan Ho Song-
dc.identifier.doi10.3349/ymj.2001.42.3.345-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00601-
dc.contributor.localIdA01793-
dc.relation.journalcodeJ02813-
dc.identifier.eissn1976-2437-
dc.identifier.pmid11456402-
dc.subject.keywordbalanced complex chromosome rearrangement-
dc.subject.keywordfluorescence in situ hybridization-
dc.contributor.alternativeNameKim, Sei Kwang-
dc.contributor.alternativeNameBai, Sang Wook-
dc.contributor.affiliatedAuthorKim, Sei Kwang-
dc.contributor.affiliatedAuthorBai, Sang Wook-
dc.rights.accessRightsfree-
dc.citation.volume42-
dc.citation.number3-
dc.citation.startPage345-
dc.citation.endPage348-
dc.identifier.bibliographicCitationYONSEI MEDICAL JOURNAL, Vol.42(3) : 345-348, 2001-
dc.identifier.rimsid31684-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers

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