Jacobs PA, Browne C, Gregson N, Joyce C, White H. Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding. J Med Genet. 1992;29:103–8.
Article CAS PubMed PubMed Central Google Scholar
Sugiura-Ogasawara M, Ozaki Y, Sato T, Suzumori N, Suzumori K. Poor prognosis of recurrent aborters with either maternal or paternal reciprocal translocations. Fertil Steril. 2004;81:367–73.
Madan K, Nieuwint AW, van Bever Y. Recombination in a balanced complex translocation of a mother leading to a balanced reciprocal translocation in the child. Review of 60 cases of balanced complex translocations. Hum Genet. 1997;99:806–15.
Article CAS PubMed Google Scholar
Ogilvie CM, Braude P, Scriven PN. Successful pregnancy outcomes after preimplantation genetic diagnosis (PGD) for carriers of chromosome translocations. Hum Fertil (Camb). 2001;4:168–71.
Article CAS PubMed Google Scholar
Kato K, Aoyama N, Kawasaki N, Hayashi H, Xiaohui T, Abe T, et al. Reproductive outcomes following preimplantation genetic diagnosis using fluorescence in situ hybridization for 52 translocation carrier couples with a history of recurrent pregnancy loss. J Hum Genet. 2016;61:687–92.
Article CAS PubMed Google Scholar
Kurahashi H, Kato T, Miyazaki J, Nishizawa H, Nishio E, Furukawa H, et al. Preimplantation genetic diagnosis/screening by comprehensive molecular testing. Reprod Med Biol. 2016;15:13–19.
Article CAS PubMed Google Scholar
Tulay P, Gultomruk M, Findikli N, Yagmur E, Bahceci M. Is the interchromosomal effect present in embryos derived from Robertsonian and reciprocal translocation carriers particularly focusing on chromosome 10 rearrangements? Zygote 2015;23:908–15.
Article CAS PubMed Google Scholar
Bartels CB, Makhijani R, Godiwala P, Bartolucci A, Nulsen JC, Grow DR, et al. In vitro fertilization outcomes after preimplantation genetic testing for chromosomal structural rearrangements comparing fluorescence in-situ hybridization, microarray comparative genomic hybridization, and next-generation sequencing. F S Rep. 2020;1:249–56.
PubMed PubMed Central Google Scholar
Nakano T, Ammae M, Satoh M, Mizuno S, Nakaoka Y, Morimoto Y. Analysis of clinical outcomes and meiotic segregation modes following preimplantation genetic testing for structural rearrangements using aCGH/NGS in couples with balanced chromosome rearrangement. Reprod Med Biol. 2022;21:e12476.
Article CAS PubMed PubMed Central Google Scholar
Viotti M. Preimplantation genetic testing for chromosomal abnormalities: aneuploidy, mosaicism, and structural rearrangements. Genes. 2020;11:602.
Article CAS PubMed PubMed Central Google Scholar
Bono S, Biricik A, Spizzichino L, Nuccitelli A, Minasi MG, Greco E, et al. Validation of a semiconductor next-generation sequencing-based protocol for preimplantation genetic diagnosis of reciprocal translocations. Prenat Diagn. 2015;35:938–44.
Article CAS PubMed Google Scholar
Iwasa T, Kuwahara A, Takeshita T, Taniguchi Y, Mikami M, Irahara M. Preimplantation genetic testing for aneuploidy and chromosomal structural rearrangement: a summary of a nationwide study by the Japan Society of Obstetrics and Gynecology. Reprod Med Biol. 2023;22:e12518.
Article PubMed PubMed Central Google Scholar
Kato K, Kuroda T, Yamadera-Egawa R, Ezoe K, Aoyama N, Usami A, et al. Preimplantation genetic testing for aneuploidy for recurrent pregnancy loss and recurrent implantation failure in minimal ovarian stimulation cycle for women aged 35-42 years: live birth rate, developmental follow-up of children, and embryo ranking. Reprod Sci. 2023;30:974–83.
Article CAS PubMed Google Scholar
Takeuchi K. Pre-implantation genetic testing: past, present, future. Reprod Med Biol. 2021;20:27–40.
Sato T, Sugiura-Ogasawara M, Ozawa F, Yamamoto T, Kato T, Kurahashi H, et al. Preimplantation genetic testing for aneuploidy: a comparison of live birth rates in patients with recurrent pregnancy loss due to embryonic aneuploidy or recurrent implantation failure. Hum Reprod. 2019;34:2340–8.
Ma X, Xu X, Mao B, Liu H, Li H, Liu K, et al. Chromosomal analysis for embryos from balanced chromosomal rearrangement carriers using next generation sequencing. Mol Reprod Dev. 2021;88:362–70.
Article CAS PubMed Google Scholar
Shetty S, Nair J, Johnson J, Shetty N, Kumar AJ, Thondehalmath N, et al. Preimplantation genetic testing for couples with balanced chromosomal rearrangements. J Reprod Infertil. 2022;23:213–23.
PubMed PubMed Central Google Scholar
Park SJ, Min JY, Kang JS, Yang BG, Hwang SY, Han SH. Chromosomal abnormalities of 19,000 couples with recurrent spontaneous abortions: a multicenter study. Fertil Steril. 2022;117:1015–25.
Article CAS PubMed Google Scholar
Ogur C, Kahraman S, Griffin DK, Cinar Yapan C, Tufekci MA, Cetinkaya M, et al. PGT for structural chromosomal rearrangements in 300 couples reveals specific risk factors but an interchromosomal effect is unlikely. Reprod Biomed Online. 2023;46:713–27.
Article CAS PubMed Google Scholar
Xie Y, Xu Y, Wang J, Miao B, Zeng Y, Ding C, et al. Preliminary analysis of numerical chromosome abnormalities in reciprocal and Robertsonian translocation preimplantation genetic diagnosis cases with 24-chromosomal analysis with an aCGH/SNP microarray. J Assist Reprod Genet. 2018;35:177–86.
Grande M, Borrell A, Garcia-Posada R, Borobio V, Muñoz M, Creus M, et al. The effect of maternal age on chromosomal anomaly rate and spectrum in recurrent miscarriage. Hum Reprod. 2012;27:3109–17.
Yuan P, Zheng L, Ou S, Zhao H, Li R, Luo H, et al. Evaluation of chromosomal abnormalities from preimplantation genetic testing to the reproductive outcomes: a comparison between three different structural rearrangements based on next-generation sequencing. J Assist Reprod Genet. 2021;38:709–18.
Article PubMed PubMed Central Google Scholar
Estop AM, Cieply K, Munne S, Surti U, Wakim A, Feingold E. Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies. Hum Genet. 2000;106:517–24.
Article CAS PubMed Google Scholar
Miller DE. The interchromosomal effect: different meanings for different organisms. Genetics. 2020;216:621–31.
Article CAS PubMed PubMed Central Google Scholar
Boynukalin FK, Gultomruk M, Turgut NE, Rubio C, Rodrigo L, Yarkiner Z, et al. The impact of patient, embryo, and translocation characteristics on the ploidy status of young couples undergoing preimplantation genetic testing for structural rearrangements (PGT-SR) by next generation sequencing (NGS). J Assist Reprod Genet. 2021;38:387–96.
Article PubMed PubMed Central Google Scholar
Fan J, Zhang X, Chen Y, Zhang J, Zhang L, Bi X, et al. Exploration of the interchromosomal effects in preimplantation genetic testing for structural rearrangements based on next-generation sequencing. Mol Genet Genom Med. 2022;10:e2017.
Mayeur A, Ahdad N, Hesters L, Grynberg M, Romana S, Sonigo C, et al. Does the prognosis after PGT for structural rearrangement differ between female and male translocation carriers? Reprod Biomed Online. 2020;40:684–92.
Article CAS PubMed Google Scholar
Wang J, Li D, Xu Z, Diao Z, Zhou J, Lin F, et al. Analysis of meiotic segregation modes in biopsied blastocysts from preimplantation genetic testing cycles of reciprocal translocations. Mol Cytogenet. 2019;12:11.
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