Partial Trisomy 1q41-qter and Partial Trisomy 9pter-9q21.32 in a Newborn Infant: An Array CGH Analysis and Review

dc.authorid0000-0002-0583-4683
dc.authorid0000-0002-7487-4603
dc.authorid0000-0003-1438-2081
dc.contributor.authorAkalin, Ibrahim
dc.contributor.authorBozdag, Senol
dc.contributor.authorSpielmann, Malte
dc.contributor.authorBasaran, Sarenur Yilmaz
dc.contributor.authorNanda, Indrajit
dc.contributor.authorKlopocki, Eva
dc.date.accessioned2025-05-10T19:53:30Z
dc.date.issued2014
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractWe report on a girl who presented with distinctive abducted hip and hyperextended knee. Cytogenetic analysis detected an extra derivative chromosome resulting from a balanced translocation in the mother and 3:1 segregation. Using array comparative genomic hybridization (CGH) in combination with conventional high resolution GTG banding, we designate the karyotype as 47, XX, +der(9)t(1;9)(q41;q21.32)mat, indicating tertiary trisomy of chromosome segments 1q41-qter and 9pter-9q21.32. A review and genotype-phenotype correlation suggested that the patient represented most of the manifestations of duplication of chromosome arms 1q and 9p. To our knowledge, a similar case has so far not been reported. (c) 2013 Wiley Periodicals, Inc.
dc.identifier.doi10.1002/ajmg.a.36278
dc.identifier.endpage494
dc.identifier.issn1552-4825
dc.identifier.issn1552-4833
dc.identifier.issue2
dc.identifier.pmid24311106
dc.identifier.scopus2-s2.0-84892874401
dc.identifier.scopusqualityQ3
dc.identifier.startpage490
dc.identifier.urihttps://doi.org/10.1002/ajmg.a.36278
dc.identifier.urihttps://hdl.handle.net/20.500.14730/12757
dc.identifier.volume164
dc.identifier.wosWOS:000331067100032
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley-Blackwell
dc.relation.ispartofAmerican Journal of Medical Genetics Part A
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectt(1
dc.subject9)
dc.subjectduplication 1q41
dc.subjectduplication 9p
dc.subjectpartial trisomy
dc.subjectarray CGH
dc.titlePartial Trisomy 1q41-qter and Partial Trisomy 9pter-9q21.32 in a Newborn Infant: An Array CGH Analysis and Review
dc.typeArticle

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