References

  1. Larsen EC, Christiansen OB, Kolte AM, Macklon N. New insights into mechanisms behind miscarriage. BMC Medicine. 2013;11:154. PubMed | Google Scholar

  2. Dutta UR, Rajitha P, Pidugu VK, Dalal AB. Cytogenetic abnormalities in 1162 couples with recurrent miscarriages in Southern region of India: report and review. Journal of assisted reproduction and genetics. 2011;28(2):145-9. PubMed | Google Scholar

  3. Elghezal H, Hidar S, Mougou S, Khairi H, Saâd A. Prevalence of chromosomal abnormalities in couples with recurrent miscarriage. Fertility and Sterility. 2007; 88 (3):721-3. PubMed | Google Scholar

  4. Merviel P, Lanta S, Allier G, Gagneur O, Najas S, Nasreddine A et al. Avortements spontanés à répétition. EMC-Gynecologie-Obstetrique. 2005;2(3):278-96. Google Scholar

  5. Jauniaux E, Farquharson RG, Christiansen OB, Exalto N. Evidence-based guidelines for the investigation and medical treatment of recurrent miscarriage. Human Reproduction. 2006; 21 (9):2216-22. PubMed | Google Scholar

  6. Ford HB, Schust DJ. Recurrent pregnancy loss: etiology, diagnosis, and therapy. Reviews in Obstetrics and Gynecology. 2009 Spring;2(2):76-83. PubMed | Google Scholar

  7. Branch DW, Gibson M, Silver RM. Recurrent miscarriage. New England Journal of Medicine. 2010;363(18):1740-7. PubMed | Google Scholar

  8. Lee J, Oh J, Choi E, Park I, Han C, Choi B-C et al. Differentially expressed genes implicated in unexplained recurrent spontaneous abortion . The International Journal of Biochemistry & Cell Biology. 2007; 39(12):2265-77. PubMed | Google Scholar

  9. Toth B, Jeschke U, Rogenhofer N, Scholz C, Würfel W, Thaler CJ et al. Recurrent miscarriage: current concepts in diagnosis and treatment. Journal of Reproductive Immunology. 2010; 85 (1):25-32. PubMed | Google Scholar

  10. Jaslow CR, Carney JL, Kutteh WH. Diagnostic factors identified in 1020 women with two versus three or more recurrent pregnancy losses. Fertility and Sterility. 2010;93(4):1234-43. PubMed | Google Scholar

  11. Dutta UR, Ponnala R, Dalal A. A novel de novo balanced reciprocal translocation t (18; 22) associated with recurrent miscarriages: a case report. J Reprod Infertil. 2014 Apr;15(2):113-6. PubMed | Google Scholar

  12. Flynn H, Yan J, Saravelos SH, Li TC. Comparison of reproductive outcome, including the pattern of loss, between couples with chromosomal abnormalities and those with unexplained repeated miscarriages. Journal of Obstetrics and Gynaecology Research. 2013; 40 (1):109-16. PubMed | Google Scholar

  13. Carp H, Feldman B, Oelsner G, Schiff E. Parental karyotype and subsequent live births in recurrent miscarriage. Fertility and Sterility. 2004; 81 (5):1296-301. PubMed | Google Scholar

  14. Byrne JL, Ward K. Genetic factors in recurrent abortion. Clinical Obstetrics and Gynecology. 1994; 37 (3):693-704. PubMed | Google Scholar

  15. Mozdarani H, Meybodi AM, Zari-Moradi S. A cytogenetic study of couples with recurrent spontaneous abortions and infertile patients with recurrent IVF/ICSI failure. Indian Journal of Human Genetics. 2008; 14 (1):1. PubMed | Google Scholar

  16. Stephenson MD, Sierra S. Reproductive outcomes in recurrent pregnancy loss associated with a parental carrier of a structural chromosome rearrangement. Human Reproduction. 2006;21 (4):1076-82. PubMed | Google Scholar

  17. Frikha R, Bouayed NA, Rebai T. Prévalence des anomalies cytogénétiques parentales au cours de l'avortement spontané récurrent: à propos de 168 couples. Immuno-analyse & Biologie Spécialisée. 2012; 27 (5):223-32. Google Scholar

  18. Asgari A, Ghahremani S, Saeedi S, Kamrani E. The study of chromosomal abnormalities and heteromorphism in couples with 2 or 3 recurrent abortions in Shahid Beheshti Hospital of Hamedan. Iranian journal of Reproductive Medicine. 2013; 11 (3):201. PubMed | Google Scholar

  19. Mogib El-Dahtory FA. Chromosomal abnormalities as a cause of recurrent abortions in Egypt. Indian J Hum Genet. 2011 May;17(2):82-4. Google Scholar

  20. Baghbani F, Mirzaee S, Hassanzadeh-Nazarabadi M. Association of heteromorphism of chromosome 9 and recurrent abortion (ultrasound diagnosed blighted ovum): a case report. Iranian Journal of Reproductive Medicine. 2014; 12 (5):357. PubMed | Google Scholar

  21. Wang Y-W, Han W-T, Guan C-J, Ge W, Zhu X-Q, Jiang M et al. Cytogenetic Study on Couples with a History of Reproductive Failure in China. Journal of Reproduction and Contraception. 2009; 20 (4):237-46. Google Scholar

  22. Goddijn M, Leschot N. Genetic aspects of miscarriage. Best Practice & Research Clinical Obstetrics & Gynaecology. 2000; 14 (5):855-65. PubMed | Google Scholar

  23. Fryns J-P, Van Buggenhout G. Structural chromosome rearrangements in couples with recurrent fetal wastage. European Journal of Obstetrics & Gynecology and Reproductive Biology. 1998; 81 (2):171-6. PubMed | Google Scholar

  24. Uehara S, Akai Y, Takeyama Y, Takabayashi T, Okamura K, Yajima A. Pericentric inversion of chromosome 9 in prenatal diagnosis and infertility. The Tohoku Journal of Experimental Medicine. 1992; 166 (4):417-27. PubMed | Google Scholar

  25. Rodriguez-Gómez MT, Martín-Sempere MJ, Abrisqueta J. C-band length variability and reproductive wastage. Human Genetics. 1987; 75 (1):56-61. PubMed | Google Scholar

  26. Genest P. Chromosome variants and abnormalities detected in 51 married couples with repeated spontaneous abortions. Clinical Genetics. 1979; 16 (6):387-9. PubMed | Google Scholar

  27. Goddijn M, Joosten J, Knegt A, Franssen M, Bonsel G, Leschot N. Clinical relevance of diagnosing structural chromosome abnormalities in couples with repeated miscarriage. Human Reproduction. 2004; 19 (4):1013-7. PubMed | Google Scholar