Partial Trisomy 1q41-qter and Partial Trisomy 9pter-9q21.32 in a Newborn Infant: An Array CGH Analysis and Review
| dc.authorid | 0000-0002-0583-4683 | |
| dc.authorid | 0000-0002-7487-4603 | |
| dc.authorid | 0000-0003-1438-2081 | |
| dc.contributor.author | Akalin, Ibrahim | |
| dc.contributor.author | Bozdag, Senol | |
| dc.contributor.author | Spielmann, Malte | |
| dc.contributor.author | Basaran, Sarenur Yilmaz | |
| dc.contributor.author | Nanda, Indrajit | |
| dc.contributor.author | Klopocki, Eva | |
| dc.date.accessioned | 2025-05-10T19:53:30Z | |
| dc.date.issued | 2014 | |
| dc.department | İstanbul Medeniyet Üniversitesi | |
| dc.description.abstract | We 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.doi | 10.1002/ajmg.a.36278 | |
| dc.identifier.endpage | 494 | |
| dc.identifier.issn | 1552-4825 | |
| dc.identifier.issn | 1552-4833 | |
| dc.identifier.issue | 2 | |
| dc.identifier.pmid | 24311106 | |
| dc.identifier.scopus | 2-s2.0-84892874401 | |
| dc.identifier.scopusquality | Q3 | |
| dc.identifier.startpage | 490 | |
| dc.identifier.uri | https://doi.org/10.1002/ajmg.a.36278 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14730/12757 | |
| dc.identifier.volume | 164 | |
| dc.identifier.wos | WOS:000331067100032 | |
| dc.identifier.wosquality | Q3 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | Wiley-Blackwell | |
| dc.relation.ispartof | American Journal of Medical Genetics Part A | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_WOS_20250302 | |
| dc.subject | t(1 | |
| dc.subject | 9) | |
| dc.subject | duplication 1q41 | |
| dc.subject | duplication 9p | |
| dc.subject | partial trisomy | |
| dc.subject | array CGH | |
| dc.title | Partial Trisomy 1q41-qter and Partial Trisomy 9pter-9q21.32 in a Newborn Infant: An Array CGH Analysis and Review | |
| dc.type | Article |










