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dc.creatorGuc-Scekić, M
dc.creatorMilašin, Jelena
dc.creatorStevanović, Milena
dc.creatorStojanov, LJ
dc.creatorĐorđević, M
dc.date.accessioned2022-11-15T13:36:21Z
dc.date.available2022-11-15T13:36:21Z
dc.date.issued2002
dc.identifier.issn0009-9163
dc.identifier.urihttps://imagine.imgge.bg.ac.rs/handle/123456789/170
dc.description.abstractLiveborn infants with tetraploidy are very rare in human pregnancies and usually die during the first days or months. Seven cases of liveborn infants with tetraploidy have previously been reported. Among them only two 92, XXXX infants survived for longer than 12 months. Here we report on the case of a 26-month-old girl with tetraploidy. The main clinical features of tetraploidy are facial dysmorphism, severely delayed growth and developmental delay. On the basis of molecular studies we discuss the possible origin of the additional chromosome sets in our proband. To our knowledge, this infant is the first reported case of tetraploidy who lived up to 26 months.en
dc.publisherWiley, Hoboken
dc.rightsrestrictedAccess
dc.sourceClinical Genetics
dc.subjecthumansen
dc.subjectconstitutive tetraploidyen
dc.titleTetraploidy in a 26-month-old girl (cytogenetic and molecular studies)en
dc.typearticle
dc.rights.licenseARR
dc.citation.epage65
dc.citation.issue1
dc.citation.other61(1): 62-65
dc.citation.rankM22
dc.citation.spage62
dc.citation.volume61
dc.identifier.doi10.1034/j.1399-0004.2002.610112.x
dc.identifier.pmid11903358
dc.identifier.scopus2-s2.0-0036461305
dc.identifier.wos000174828700015
dc.type.versionpublishedVersion


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