Uysal, AhmetUludağ, A.Sılan, FatmaErcelen, N.Zafer, C.Ozdemir, O.2025-01-272025-01-2720131311-0160https://doi.org/10.2478/bjmg-2013-0022https://hdl.handle.net/20.500.12428/22126Double 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.eninfo:eu-repo/semantics/openAccessDouble translocationRobertsonian translocationFluorescent in situ hybridization (FISH)Miscar-riageArticle161778010.2478/bjmg-2013-0022Q4WOS:0003257179000112-s2.0-8490125678824265590Q4