DOUBLE TRANSLOCATION: AN INTERESTING FAMILY HISTORY

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dc.contributor.authorUysal, Ahmet
dc.contributor.authorUludağ, A.
dc.contributor.authorSılan, Fatma
dc.contributor.authorErcelen, N.
dc.contributor.authorZafer, C.
dc.contributor.authorOzdemir, O.
dc.date.accessioned2025-01-27T20:23:07Z
dc.date.available2025-01-27T20:23:07Z
dc.date.issued2013
dc.departmentÇanakkale Onsekiz Mart Üniversitesi
dc.description.abstractDouble balanced translocations are particularly rare and the risk of a fetus with an unbalanced chromosomal anomaly is greater than for single translocation carriers. In this present case, we describe an interesting family history which included three generations. A couple, married for 4 years, was referred to the genetic clinic due to infertility and family chromosome anomalies. A GTG-band chromosome analysis indicated that the male partner's karyotype was 45, XY, t(3; 18)(q11; ptel)t(13; 14)(q10; q10). The same double balanced translocation was found in two others family members.
dc.identifier.doi10.2478/bjmg-2013-0022
dc.identifier.endpage80
dc.identifier.issn1311-0160
dc.identifier.issue1
dc.identifier.pmid24265590
dc.identifier.scopus2-s2.0-84901256788
dc.identifier.scopusqualityQ4
dc.identifier.startpage77
dc.identifier.urihttps://doi.org/10.2478/bjmg-2013-0022
dc.identifier.urihttps://hdl.handle.net/20.500.12428/22126
dc.identifier.volume16
dc.identifier.wosWOS:000325717900011
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherMacedonian Acad Sciences Arts
dc.relation.ispartofBalkan Journal of Medical Genetics
dc.relation.publicationcategoryinfo:eu-repo/semantics/openAccess
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20250125
dc.subjectDouble translocation
dc.subjectRobertsonian translocation
dc.subjectFluorescent in situ hybridization (FISH)
dc.subjectMiscar-riage
dc.titleDOUBLE TRANSLOCATION: AN INTERESTING FAMILY HISTORY
dc.typeArticle

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