[1. Rowe PJ, Comhaire FH. World Health Organization manual for the standardised investigation and diagnosis of infertile couples. Current practices and controversies in assisted reproduction. Cambridge, UK: Cambridge University Press. 2002: 14-15.]Search in Google Scholar
[2. Azimi C, Khaleghian M, Farzanfar F. A retrospective chromosome studies among Iranian infertile women: Report of 21 years. Iran J Reprod Med. 2013; 11(4): 315-324.]Search in Google Scholar
[3. Taylor A, Braude P. ABC of subfertility. Extent of the problem. BMJ Publishing Group. 2008: 1-4.]Search in Google Scholar
[4. Dada R, Gupta NP, Kucheria K. Cytogenetic and molecular analysis of male infertility. Cell Biochem Biophys. 2006; 44(1): 171-177.10.1385/CBB:44:1:171]Search in Google Scholar
[5. Akgul M, Ozkinay F, Ercal D. Cytogenetic abnormalities in 179 cases with male infertility in western region of Turkey: Report and review. J Assist Reprod Genet. 2009; 6(2-3): 119-122.10.1007/s10815-009-9296-8]Search in Google Scholar
[6. Balkan M, Tekes S, Gedik A. Cytogenetic and Y chromosome microdeletion screening studies in infertile males with oligozoospermia and azoospermia in Southeast Turkey. J Assist Reprod Genet. 2008; 25(11-12): 559-565.10.1007/s10815-008-9272-8]Search in Google Scholar
[7. Azimi C, Khaleghian M, Farzanfar F. Cytogenetic studies among Iranian infertile men: The first 20-year long-term report. Afr J Biotechnol. 2012; 11(37): 8973-8978.10.5897/AJB12.650]Search in Google Scholar
[8. Clementini E, Palka C, Iezzi I, Stuppia L, Guanciali- Franchi P, Tiboni GM. Prevalence of chromosomal abnormalities in 2078 infertile couples referred for assisted reproductive techniques. Hum Reprod. 2005; 20(2): 4327-4442.10.1093/humrep/deh626]Search in Google Scholar
[9. Rosenbusch B. Somatic chromosomal abnormalities in couples undergoing infertility treatment by intracytoplasmic sperm injection. J Genet. 2010; 89(1): 105-108.10.1007/s12041-010-0002-5]Search in Google Scholar
[10. Gekas J, Thepot F, Turleau C, Siffroi JP, Dadoune JP, Wasels R, et al. Chromosomal factors of infertility in candidate couples for ICSI: An equal risk of constitutional aberration in women and men. Hum Reprod. 2001; 16(1): 82-90.10.1093/humrep/16.1.82]Search in Google Scholar
[11. Gersen SL, Keagle MB. Human chromosome nomenclature. An overview and definition in terms. The Principles of Clinical Cytogenetics. Totowa, New Jersey: Humana Press. 2005: 541-544.]Search in Google Scholar
[12. Elghezal H, Hidar S, Braham R, Denguezli W, Ajina M, Saâd A. Chromosome abnormalities in one thousand infertile males with nonobstructive sperm disorders. Fertil Steril. 2006; 86(6): 1792-1795.10.1016/j.fertnstert.2006.04.041]Search in Google Scholar
[13. Raziel A, Friedler S, Schachter M, Kastertein E, Strassburger D, Ron-El R. Increased frequency of female partner chromosomal abnormalities in patients with high-order implantation failure after in vitro fertilization. Fertil Steril. 2002; 78(3): 515-519.10.1016/S0015-0282(02)03298-3]Search in Google Scholar
[14. Yatsenko AN, Yatsenko SA, Weedin JW, Lawrence AE, Patel A, Peacock S, et al. Comprehensive 5-year study of cytogenetic aberrations in 668 infertile men. J Urol. 2010; 183(4): 1632-1642.10.1016/j.juro.2009.12.004]Search in Google Scholar
[15. Ravel C, Berthant I, Bresson JL, Siffroi JP. Prevalence of chromosomal abnormalities in phenotypically normal and fertile adult males: Large-scale survey for over 10000 sperm donor karyotypes. Hum Reprod. 2006; 21(6): 1484-1489.10.1093/humrep/del024]Search in Google Scholar
[16. Vicdan A, Vicdan K, Gunalp S, Kence A, Akarsu C, Isik AZ, et al. Genetic aspects of human male infertility: The frequencies of chromosomal abnormalities and Y chromosome microdeletions in severe male factor infertility. Eur J Obstet Gynecol Reprod Biol. 204; 117(1): 49-54.10.1016/j.ejogrb.2003.07.006]Search in Google Scholar
[17. Shaffer LG, McGowan J, Schmid M. ISCN 2013 An international system for human cytogenetic nomenclature. Published in collaboration with Cytogenetic and Genome Research, Karger, 2013.]Search in Google Scholar
[18. Al-Achkar W, Wafa A, Moassass F. Cytogenetic abnormalities and Y-chromosome microdeletions in infertile Syrian males. Biomed Reports. 2013; 1(2): 275-279.10.3892/br.2012.40]Search in Google Scholar
[19. Jungwirth A, Diemer T, Dohle GR, Giwercman A, Kopa Z, Krausz C, et al. Guidelines on Male Infertility. European Association of Urology, 2012.]Search in Google Scholar
[20. Scriven PN, Flinter FA, Braude PR, Ogilvie CM. Robertsonian translocations ‒ Reproductive risks and indications for preimplantation genetic diagnosis. Hum Reprod. 2001; 16(11): 2267-2273.10.1093/humrep/16.11.2267]Search in Google Scholar
[21. Bellovits O, Rusz A, Romics I, Csonka E, Hadlaczky G. Chromosomal aneuploidy in azoospermic men. PéterInt J Hum Genet. 2006; 6(2): 171-176.10.1080/09723757.2006.11885959]Search in Google Scholar
[22. Lanfranco F, Kamischke A, Zitzmann M, Nieschlag E. Klinefelter’s syndrome. Lancet. 2004; 364(9430): 273-283.10.1016/S0140-6736(04)16678-6]Search in Google Scholar
[23. Mierla D, Jardan D, Stoian V. Chromosomal abnormality in men with impaired spermatogenesis. Int J Fertil Steril. 2014; 8(1): 35-42.]Search in Google Scholar
[24. Poongothai J, Gopenath TS, Manonayaki S. Genetics of human male fertility. Singapore Med J. 2009; 50(4): 336-347.]Search in Google Scholar
[25. Mozdarani H, Mohseni Meybody A, Zari-Moradi S. A cytogenetic study of couples with recurrent spontaneous abortions and infertile patients with recurrent IVF/ICSI failure. Indian J Hum Genet. 2008; 14(1): 1-6.10.4103/0971-6866.42319284078120300283]Search in Google Scholar
[26. Guimarães J, Almeida Santos T, Barbosa A, Bastos M, Almeida Santos A, Carvalheiro M. Screening for gene SRY by FISH in patients with Turner syndrome. Endocrine Abstracts. 2006; 11P: 720. ]Search in Google Scholar