Publication:
Familial T(1;17) Balanced Translocation Carrier with Mental Retardation and Epilepsy Cases: Scientific Letter

dc.authorscopusid6603432100
dc.authorscopusid6603455076
dc.authorscopusid18038193800
dc.authorscopusid6601981559
dc.authorscopusid51562717700
dc.authorscopusid12805499100
dc.authorscopusid12805499100
dc.contributor.authorGüneş, S.
dc.contributor.authorKara, N.
dc.contributor.authorÖkten, G.
dc.contributor.authorTaşdemir, H.A.
dc.contributor.authorTürkeli Sezer, Ö.
dc.contributor.authorYigit, S.
dc.contributor.authorOgur, G.
dc.date.accessioned2025-12-10T21:33:30Z
dc.date.issued2008
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Güneş] Sezgin Özgür, Tibbi Genetik BD, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Genetik BD, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Kara] Nurten, Tibbi Genetik BD, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ökten] Gülsen, Tibbi Genetik BD, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Taşdemir] Haydar Ali, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Türkeli Sezer] Özlem, Tibbi Genetik, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Yigit] Serbulent, Tibbi Genetik, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ogǔr] Gönül, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractReciprocal translocations, the most frequent structural aberration in humans, are mainly transmitted by one of the parents. Balanced reciprocal translocations occur at a frequency of approximately 1 in 600 live births. Familial reciprocal translocations are generally without phenotypic effect, although there is some evidence for a small excess of mental retardation (MR) in children carrying familial reciprocal translocations. We describe three children presenting with moderate MR/epilepsy and a familial balanced reciprocal translocation inherited from the mother. Cytogenetic analysis of peripheral blood lymphocytes showed a balanced reciprocal translocation t(1;17)(p34;q25) in all 25 analyzed metaphase spreads. Some of the apparently balanced rearrangements associated with MR may be unbalanced at the molecular level. Further detailed molecular analysis is required to characterize these breakpoints. Copyright © 2008 by Türkiye Klinikleri.en_US
dc.identifier.endpage86en_US
dc.identifier.issn1300-0292
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-41149130248
dc.identifier.scopusqualityQ4
dc.identifier.startpage83en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12712/34721
dc.identifier.volume28en_US
dc.language.isotren_US
dc.publisherTurkiye Kliniklerien_US
dc.relation.ispartofTurkiye Klinikleri Journal of Medical Sciencesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGeneticen_US
dc.subjectEpilepsyen_US
dc.subjectMental Retardationen_US
dc.subjectTranslocationen_US
dc.titleFamilial T(1;17) Balanced Translocation Carrier with Mental Retardation and Epilepsy Cases: Scientific Letteren_US
dc.title.alternativeAilesel t(1;17) Dengeli Translokasyon Taşıyıcısı Üç Mental Retardasyon ve Epilepsi Olgusuen_US
dc.typeArticleen_US
dspace.entity.typePublication

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