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Article: Monozygotic dichorionic twins heterokaryotypic for duplication chromosome 2q13-q23.3

TitleMonozygotic dichorionic twins heterokaryotypic for duplication chromosome 2q13-q23.3
Authors
Leung, WCChoi, HLau, WLNg, LKLau, ETLo, FMChoy, KWLau, TKTang, MHYChin, R
KeywordsChromosome duplication
Heterokaryotype
Twins, dichorionic, monozygotic
Issue Date2009
PublisherS Karger AG. The Journal's web site is located at http://www.karger.com/FDT
Citation
Fetal Diagnosis And Therapy, 2009, v. 25 n. 4, p. 397-399 How to Cite?
DOI: http://dx.doi.org/10.1159/000236153
AbstractWe present an evaluation of the diagnosis, management and outcome of a pair of heterokaryotypic monozygotic dichorionic twins. The heterokaryotype was an incidental finding from an amniocentesis performed for prenatal diagnosis of β-thalassaemia major in a pair of dichorionic twins. Monozygocity was revealed by QF-PCR showing identical short tandem repeat markers on chromosomes 21, 18, 13, X and Y. The twins were heterokaryotypic for duplication chromosome 2q13-q23.3, as shown by array comparative genomic hybridization. Selective foeticide was performed. This case demonstrates that heterokaryotypic monozygotic dichorionic twins are a genetic possibility that does occur. Copyright © 2009 S. Karger AG.
Persistent Identifierhttp://hdl.handle.net/10722/180695
ISSN
1015-3837
2023 Impact Factor: 1.6
2023 SCImago Journal Rankings: 0.767
ISI Accession Number ID
WOS:000270365300006
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorLeung, WCen_US
dc.contributor.authorChoi, Hen_US
dc.contributor.authorLau, WLen_US
dc.contributor.authorNg, LKen_US
dc.contributor.authorLau, ETen_US
dc.contributor.authorLo, FMen_US
dc.contributor.authorChoy, KWen_US
dc.contributor.authorLau, TKen_US
dc.contributor.authorTang, MHYen_US
dc.contributor.authorChin, Ren_US
dc.date.accessioned2013-01-28T01:41:11Z-
dc.date.available2013-01-28T01:41:11Z-
dc.date.issued2009en_US
dc.identifier.citationFetal Diagnosis And Therapy, 2009, v. 25 n. 4, p. 397-399en_US
dc.identifier.issn1015-3837en_US
dc.identifier.urihttp://hdl.handle.net/10722/180695-
dc.description.abstractWe present an evaluation of the diagnosis, management and outcome of a pair of heterokaryotypic monozygotic dichorionic twins. The heterokaryotype was an incidental finding from an amniocentesis performed for prenatal diagnosis of β-thalassaemia major in a pair of dichorionic twins. Monozygocity was revealed by QF-PCR showing identical short tandem repeat markers on chromosomes 21, 18, 13, X and Y. The twins were heterokaryotypic for duplication chromosome 2q13-q23.3, as shown by array comparative genomic hybridization. Selective foeticide was performed. This case demonstrates that heterokaryotypic monozygotic dichorionic twins are a genetic possibility that does occur. Copyright © 2009 S. Karger AG.en_US
dc.languageengen_US
dc.publisherS Karger AG. The Journal's web site is located at http://www.karger.com/FDTen_US
dc.relation.ispartofFetal Diagnosis and Therapyen_US
dc.subjectChromosome duplication-
dc.subjectHeterokaryotype-
dc.subjectTwins, dichorionic, monozygotic-
dc.subject.meshAdulten_US
dc.subject.meshAmniocentesisen_US
dc.subject.meshChromosomes, Human, Pair 2en_US
dc.subject.meshComparative Genomic Hybridizationen_US
dc.subject.meshFemaleen_US
dc.subject.meshGene Duplicationen_US
dc.subject.meshGenetic Counselingen_US
dc.subject.meshGenetic Testingen_US
dc.subject.meshGestational Ageen_US
dc.subject.meshHumansen_US
dc.subject.meshIncidental Findingsen_US
dc.subject.meshKaryotypingen_US
dc.subject.meshPolymerase Chain Reactionen_US
dc.subject.meshPregnancyen_US
dc.subject.meshPregnancy Reduction, Multifetalen_US
dc.subject.meshPrenatal Diagnosis - Methodsen_US
dc.subject.meshTwins, Monozygotic - Geneticsen_US
dc.subject.meshBeta-Thalassemia - Diagnosis - Geneticsen_US
dc.titleMonozygotic dichorionic twins heterokaryotypic for duplication chromosome 2q13-q23.3en_US
dc.typeArticleen_US
dc.identifier.emailTang, MHY: mhytang@hkucc.hku.hken_US
dc.identifier.authorityTang, MHY=rp01701en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1159/000236153en_US
dc.identifier.pmid19786786-
dc.identifier.scopuseid_2-s2.0-70349748626en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-70349748626&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume25en_US
dc.identifier.issue4en_US
dc.identifier.spage397en_US
dc.identifier.epage399en_US
dc.identifier.isiWOS:000270365300006-
dc.publisher.placeSwitzerlanden_US
dc.identifier.scopusauthoridLeung, WC=7201504435en_US
dc.identifier.scopusauthoridChoi, H=15047739500en_US
dc.identifier.scopusauthoridLau, WL=12142218500en_US
dc.identifier.scopusauthoridNg, LK=25630698100en_US
dc.identifier.scopusauthoridLau, ET=7103086081en_US
dc.identifier.scopusauthoridLo, FM=35311589700en_US
dc.identifier.scopusauthoridChoy, KW=7005477052en_US
dc.identifier.scopusauthoridLau, TK=24491963900en_US
dc.identifier.scopusauthoridTang, MHY=8943401300en_US
dc.identifier.scopusauthoridChin, R=24358899900en_US
dc.identifier.issnl1015-3837-

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