Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/2549
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dc.contributor.authorGuc-Scekic, Marijaen_US
dc.contributor.authorMilasin, J.en_US
dc.contributor.authorStevanović, Milenaen_US
dc.contributor.authorStojanov, L. J.en_US
dc.contributor.authorDjordjevic, M.en_US
dc.date.accessioned2019-10-24T19:20:55Z-
dc.date.available2019-10-24T19:20:55Z-
dc.date.issued2002-01-
dc.identifier.issn0009-9163-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/2549-
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_US
dc.language.isoenen_US
dc.relation.ispartofClinical Geneticsen_US
dc.subjectConstitutive tetraploidyen_US
dc.subjectHumansen_US
dc.titleTetraploidy in a 26-month-old girl (cytogenetic and molecular studies)en_US
dc.typeArticleen_US
dc.identifier.doi10.1034/j.1399-0004.2002.610112.x-
dc.identifier.pmid11903358-
dc.identifier.scopus2-s2.0-0036461305-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/0036461305-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0003-4286-7334-
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