E. Larsen, O. Christiansen, A. Kolte, and N. Macklon, New insights into mechanisms behind miscarriage, BMC Medicine, vol.90, issue.1, p.154, 2013.
DOI : 10.1016/j.fertnstert.2007.07.1290
URL : https://bmcmedicine.biomedcentral.com/track/pdf/10.1186/1741-7015-11-154?site=bmcmedicine.biomedcentral.com

U. Dutta, P. Rajitha, V. Pidugu, and A. Dalal, Cytogenetic abnormalities in 1162 couples with recurrent miscarriages in Southern region of India: report and review, Journal of Assisted Reproduction and Genetics, vol.59, issue.2, 2011.
DOI : 10.1002/ajmg.1320240214

H. Elghezal, S. Hidar, S. Mougou, H. Khairi, and A. Saã¢d, Prevalence of chromosomal abnormalities in couples with??recurrent miscarriage, Fertility and Sterility, vol.88, issue.3, pp.721-724, 2007.
DOI : 10.1016/j.fertnstert.2006.11.160

P. Merviel, S. Lanta, G. Allier, O. Gagneur, S. Najas et al., Avortements spontanés à répétition. EMC-Gynecologie- Obstetrique, pp.278-96, 2005.

E. Jauniaux, R. Farquharson, O. Christiansen, and N. Exalto, Evidence-based guidelines for the investigation and medical treatment of recurrent miscarriage, Human Reproduction, vol.21, issue.9, pp.2216-2238, 2006.
DOI : 10.1093/humrep/del150

H. Ford and D. Schust, Recurrent pregnancy loss: etiology, diagnosis, and therapy. Reviews in Obstetrics and Gynecology, Spring, vol.2, issue.2, pp.76-83, 2009.

D. Branch, M. Gibson, and R. Silver, Recurrent miscarriage, New England Journal of Medicine, vol.363, 2010.

J. Lee, J. Oh, E. Choi, I. Park, C. Han et al., Differentially expressed genes implicated in unexplained recurrent spontaneous abortion, The International Journal of Biochemistry & Cell Biology, vol.39, issue.12, 2007.
DOI : 10.1016/j.biocel.2007.06.012

B. Toth, U. Jeschke, N. Rogenhofer, C. Scholz, W. Würfel et al., Recurrent miscarriage: current concepts in diagnosis and treatment, Journal of Reproductive Immunology, vol.85, issue.1, pp.25-32, 2010.
DOI : 10.1016/j.jri.2009.12.006

C. Jaslow, J. Carney, and W. Kutteh, Diagnostic factors identified in 1020 women with two versus three or more recurrent pregnancy losses, Fertility and Sterility, vol.93, issue.4, pp.1234-1277, 2010.
DOI : 10.1016/j.fertnstert.2009.01.166

U. Dutta, R. Ponnala, and A. Dalal, A novel de novo balanced reciprocal translocation t (18; 22) associated with recurrent miscarriages: a case report, J Reprod Infertil, 2014.

H. Flynn, J. Yan, S. Saravelos, and T. Li, 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, vol.26, issue.1, 2013.
DOI : 10.1093/humrep/der068

H. Carp, B. Feldman, G. Oelsner, and E. Schiff, Parental karyotype and subsequent live births in recurrent miscarriage, Fertility and Sterility, vol.81, issue.5, pp.1296-301, 2004.
DOI : 10.1016/j.fertnstert.2003.09.059

J. Byrne and K. Ward, Genetic Factors in Recurrent Abortion, Clinical Obstetrics and Gynecology, vol.37, issue.3, 1994.
DOI : 10.1097/00003081-199409000-00021

H. Mozdarani, A. Meybodi, and S. Zari-moradi, A cytogenetic study of couples with recurrent spontaneous abortions and infertile patients with recurrent IVF/ICSI failure, Indian Journal of Human Genetics, vol.14, issue.1, 2008.
DOI : 10.4103/0971-6866.42319

M. Stephenson, S. Sierra, R. Frikha, N. Bouayed, and T. Rebai, Reproductive outcomes in recurrent pregnancy loss associated with a parental carrier of a structural chromosome rearrangement, Human Reproduction, vol.21, issue.4, pp.1076-82223, 2006.
DOI : 10.2307/2531248

A. Asgari, S. Ghahremani, S. Saeedi, and E. Kamrani, 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, vol.11, issue.3, p.201, 2013.

M. El-dahtory and F. , Chromosomal abnormalities as a cause of recurrent abortions in Egypt, Indian Journal of Human Genetics, vol.17, issue.2, 2011.
DOI : 10.4103/0971-6866.86186

F. Baghbani, S. Mirzaee, and M. Hassanzadeh-nazarabadi, Association of heteromorphism of chromosome 9 and recurrent abortion (ultrasound diagnosed blighted ovum): a case report, Iranian Journal of Reproductive Medicine, vol.12, issue.5, p.357, 2014.

Y. Wang, W. Han, C. Guan, W. Ge, X. Zhu et al., Cytogenetic Study on Couples with a History of Reproductive Failure in China, Journal of Reproduction and Contraception, vol.20, issue.4, pp.237-283, 2009.
DOI : 10.1016/S1001-7844(10)60006-5

M. Goddijn and N. Leschot, Genetic aspects of miscarriage, Best Practice & Research Clinical Obstetrics & Gynaecology, vol.14, issue.5, pp.855-65, 2000.
DOI : 10.1053/beog.2000.0124

J. Fryns, V. Buggenhout, and G. , Structural chromosome rearrangements in couples with recurrent fetal wastage, European Journal of Obstetrics & Gynecology and Reproductive Biology, vol.81, issue.2, pp.171-177, 1998.
DOI : 10.1016/S0301-2115(98)00185-7

S. Uehara, Y. Akai, Y. Takeyama, T. Takabayashi, K. Okamura et al., Pericentric Inversion of Chromosome 9 in Prenatal Diagnosis and Infertility., The Tohoku Journal of Experimental Medicine, vol.166, issue.4, pp.417-444, 1992.
DOI : 10.1620/tjem.166.417

M. Rodriguez-gómez, M. Martín-sempere, and J. Abrisqueta, Cband length variability and reproductive wastage, Human Genetics, vol.75, issue.1, pp.56-61, 1987.

P. Genest, Chromosome variants and abnormalities detected in 51 married couples with repeated spontaneous abortions, Clinical Genetics, vol.35, issue.6, pp.387-396, 1979.
DOI : 10.1111/j.1399-0004.1979.tb01346.x

M. Goddijn, J. Joosten, A. Knegt, M. Franssen, G. Bonsel et al., Clinical relevance of diagnosing structural chromosome abnormalities in couples with repeated miscarriage, Human Reproduction, vol.19, issue.4, pp.1013-1020, 2004.
DOI : 10.1093/humrep/deh172