References
- 1. Beyazyurek C, Ekmekçi CG, Sağlam Y, Çinar Ç, Kahraman S. Preimplantation genetic diagnosis (PGD) for extremes-successful birth after PGD for a consanguineous couple carrying an identical balanced reciprocal translocation. Fertil Steril. 2010; 93(7): 2413.e1-2413.e5.
- 2. Conn CM, Cozzi J, Harper JC, Winston ML, Delhanty JDA. Preimplantation genetic diagnosis for couples at high risk of Down syndrome pregnancy owing to parental translocation or mosaicism. J Med Genet. 1999; 36(1): 45-50.
- 3. Çirakoğlu A, Yilmaz S, Kuru D, Tarkan-Arguden Y, Guven GS, Deviren A, et al. Structural Chromosomal Abnormalities in Couples with Recurrent Pregnancy Loss. Turkiye Klinikleri J Med Sci, 2010;30(4): 1185-1188.
- 4. De Braekeleer M, Dao TN. Cytogenetic studies in male infertility: a review. Hum Reprod. 1991; 6(2): 245-250.
- 5. Demirhan O, Pazarbaşi A, Guzel AI, Taştemir D, Yilmaz B, Kazap M, et al. The reliability of maternal serum triple screening for the prenatal diagnosis of fetal chromosomal abnormalities in Turkish women. Genet Test Molec Biomarkers. 2011; 15(10): 701-707.
- 6. Eggermann T, Schwanitz G. Genetics of Down syndrome. In: Dey S, Ed. Genetics and Etiology of Down Syndrome, Part 1. Rijeka, Croatia: InTech. 2011: 5-22.
- 7. Hassold TJ, Jacobs PA. Trisomy in man. Ann Rev Genet. 1984; 18: 69-97.
- 8. Hobbs CA, Sherman SL, Yi P, Hopkins SE, Torfs CP, Hine RJ, et al. Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down Syndrome. Am J Hum Genet. 2000; 67(3): 623-630.
- 9. Kovaleva NV. Trisomy 21 in the offspring of carriers of balanced non-contributing autosomal rearrangements: examination of interchromosomal effect and non-homologous meiotic co-orientation. In: van den Bosch A, Dubois E, Eds. New Developments in Down Syndrome Research. New York, USA: Nova Science Publishers Inc. 2012: 149-176. (ISBN: 978-1-62081-893-0. Available from: https://www.novapublishers.com/catalog/product_info.ph;?products_id=376).
- 10. Pazarbaşi A, Demirhan O, Turgut M, Guzel AI, Taştemir D. Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down Syndrome carrying the same translocation. Genet Counsel. 2008; 19(3): 301-308.
- 11. Schinzel A. Catalogue of Unbalanced Chromosome Aberrations in Man, 2nd ed. Berlin, Germany: De Gruyter, 2001.
- 12. Banzal V, Suresh S, Suresh I, Jagadeesh S, Fazal GJ. Genetic counseling in chromosomal abnormalities. J Prenat Diagn Ther. 2010; 1(1): 14-19.
- 13. Vorzanova SG, Iourov IY, Beresheva AK, Demidova IA, Monakhov VV, Kravetz VS, et al. Nondisjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down Syndrome. Tsitol Genet. 2005; 39(6): 30-36.
- 14. Hultén MA, Jonasson J, Iwarsson E, Uppal P, Vorsanova SG, Yurov YB, et al. Trisomy 21 mosaicism: we may all have a touch of Down Syndrome. Cytogenet Genome Res. 2013; 139(3): 189-192.
- 15. Hultén MA, Patel SD, Tankimanova M, Westgren M, Papadogiannakis N, Jonsson AM, et al. On the origin of trisomy 21 Down syndrome. Mol Cytogenet. 2008; 1:21.
- 16. Hultén MA, Patel S, Jonasson J, Iwarssom E. On the origin of the maternal age effect in trisomy 21 DS: the Oocyte Mosaicism Selection model. Reproduction. 2010; 139(1): 1-9.
- 17. Anton E, Vidal F, Blanco J. Role of sperm FISH in the genetic reproductive advice of structural reorganization carriers. Hum Reprod. 2007; 22(8): 2088-2092.
- 18. Gianaroli L, Magli MC, Ferraretti AP, Dunne S, Balicchia B, Escudero T, et al. Possible interchromosomal effect in embryos generated by gametes from translocation carriers. Hum Reprod. 2002; 17(12): 3201-3207.
- 19. Pujol A, Benet J, Staessen C, van Assche E, Campillo M, Egozcue J, et al. The importance of aneu-ploidy screening in reciprocal translocation carrier. Reproduction. 2006; 131(6): 1025-1035.
- 20. Kovaleva NV. Increased risk of trisomy 21 offspring in carriers of balanced non-contributing autosomal rearrangements is not explained by interchromosomal effect. Russian J Genet. 2013; 49(2): 259-268 (in Russian).