1 . Polipalli SK, Karra VK, Jindal A, Puppala M, Singh P, Rawat K, et al.. "Cytogenetic Analysis for Suspected Chromosomal Abnormalities; A Five Years Experience" . J Clin Diagn Res. 2016; 10(9): Gc01-gc5.

2 . Hanif MI, Khan A, Arif A, Shoeb E. "Cytogenetic investigation of couples with recurrent spontaneous miscarriages" . Pak J Med Sci. 2019; 35(5):1422-7.

3 . Azim M, Khan AH, Khilji ZL, Pal JA, Khurshid M. "Chromosomal abnormalities as a cause of recurrent abortions: a hospital experience" . J Pak Med Assoc. 2003; 53 (3): 117-9.

4 . Goud TM, Mohammed Al Harassi S, Khalfan Al Salmani K, Mohammed Al Busaidy S, Rajab A. "Cytogenetic studies in couples with recurrent miscarriage in the Sultanate of Oman" . Reprod Biomed Online. 2009; 18 (3): 424-9.

5 . 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. 117(1):49-54. 204.

6 . 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(1):515-519.

7 . Franssen MT, Korevaar JC, Leschot NJ, Bossuyt PM, Knegt AC, Gerssen-Schoorl KB, et al.. "Selective chromosome analysis in couples with two or more miscarriages: case-control study" . Bmj. 2005; 331(7509):137-41.

8 . Toth B, Jeschke U, Rogenhofer N, Scholz C, Würfel W, Thaler CJ, et al.. "Recurrent miscarriage: current concepts in diagnosis and treatment" . J Reprod Immunol. 2010; 85(1):25-32.

9 . Niroumanesh S, Mehdipour P, Farajpour A, Darvish S. "A cytogenetic study of couples with repeated spontaneous abortions" . Ann Saudi Med. 2011; 31(1):77-9.

10 . Ford HB, Schust DJ. "Recurrent pregnancy loss: etiology, diagnosis, and therapy" . Rev Obstet Gynecol. 2009Spring; 2(2):76-83.

11 . Yildirim ME, Karakus S, Kurtulgan HK, Baser B, Sezgin I. "The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study" . J Gynecol Obstet Hum Reprod. 2019; 48(7):521-5.

12 . Dutta UR, Rajitha P, Pidugu VK, Dalal AB. "Cytogenetic abnormalities in 1162 couples with recurrent miscarriages in southern region of India: report and review" . J Assist Reprod Genet. 2011; 28(2):145-9.

13 . 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 J Hum Genet. 2008; 14(1):1-6.

14 . Stephenson MD, Sierra S. "Reproductive outcomes in recurrent pregnancy loss associated with a parental carrier of a structural chromosome rearrangement" . Hum Reprod. 2006; 21(4):1076-82.

15 . Soltani N, Mirzaei F, Ayatollahi H. "Cytogenetic Studies of 608 Couples with Recurrent Spontaneous Abortions in Northeastern Iran" . Iran J Pathol. 2021; 16(4):418-25.

16 . Alibakhshi R, Nejati P, Hamani S, Mir-Ahadi N, Jalilian N. "Cytogenetic Analysis of 570 Couples with Recurrent Pregnancy Loss: Reporting 11 Years of Experience" . J Hum Reprod Sci. 2020; 13(3):216-20.

17 . Amiel A, Sardos-Albertini F, Fejgin MD, Sharony R, Diukman R, Bartoov B. "Interchromosomal effect leading to an increase in aneuploidy in sperm nuclei in a man heterozygous for pericentric inversion (inv 9) and C-heterochromatin" . J Hum Genet. 2001; 46(5):245-50.

18 . Demirhan O, Pazarbasi A, Suleymanova-Karahan D, Tanriverdi N, Kilinc Y. "Correlation of clinical phenotype with a pericentric inversion of chromosome 9 and genetic counseling" . Saudi Med J. 2008; 29(7):946-51.

19 . Uehara S, Akai Y, Takeyama Y, Takabayashi T, Okamura K, Yajima A. "Pericentric inversion of chromosome 9 in prenatal diagnosis and infertility" . Tohoku J Exp Med. 1992; 166(4):417-27.

20 . Fauth C, Bartels I, Haaf T, Speicher MR. "Additional dark G-band in the p-arm of chromosome 19 due to a paracentric inversion with a breakpoint in the pericentromeric heterochromatin" . Am J Med Genet. 2001; 103(2):160-2.

21 . Anuradha N, Satyanarayana M, Manjunatha KR. "Satellite Associations in Recurrent Aborters" . International Journal of Human Genetics. 2002; 2(1):61-4.

22 . Rodriguez-Gómez MT, Martín-Sempere MJ, Abrisqueta JA. "C-band length variability and reproductive wastage" . Hum Genet. 1987; 75(1):56-61.

23 . Kalantari P, Sepehri H, Behjati F, Ashtiani ZO, Akbari MT. "Chromosomal studies in infertile men" , Tsitol Genet, 2001, vol. 35 (pg. 50-54).

24 . Boronova I, Bernasovska J, Cakanova G, Ferenc P, Petrejcikova E, Szabadosova V. "Heterochromatin Variants in Slovak Women with Reproductive Failure" . International Journal of Human Genetics. 2015; 15(1):1-5.

25 . Caglayan A.O., Ozyazgan I, Demiryilmaz F, Ozgun M.T. "Are heterochromatin polymorphisms associated with recurrent miscarriage?" J Obstet Gynaecol Res, 36 (4) (2010), pp. 774-776.

26 . De la Fuente-Cortés BE, Cerda-Flores RM, Dávila-Rodríguez MI, Garcí-Vielma C, De la Rosa Alvarado RM, Cortés-Gutiérrez EI. "Chromosomal abnormalities and polymorphic variants in couples with repeated miscarriage in Mexico" . Reprod Biomed Online. 2009Apr; 18(4):543-8.

27 . El-Dahtory F., Yahia S., Rasheed R.A., & Wahba Y. (2022). "Prevalence and patterns of chromosomal abnormalities among Egyptian patients with infertility: a single institution's 5-year experience" . Middle East Fertility Society Journal, 27(1), 1-5.

28 . 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.