[1] Bielanska, M., Tan, S.L., Ao, A., 2000. Fluorescence in-situ hybridization of sex chromosomes in spermatozoa and spare preimplantation embryos of a Klinefelter 46, XY/47, XXY male. Hum Reprod, 15:440-444.

[2] Jin, F., Shi, Y.F., Zhou, F.Z., Huang, H.F., 1998. Influence of sperm quality and quantity on fertilization, cleavage rates and quality of embryos in in-vitro fertilization. Chin J Obstet Gynecol., 33:28-30 (in Chinese).

[3] Gianaroli, L., Magli, M.C., Ferraretti, A.P., Fiorentino, A., Garrisi, J., Munne, S., 1997. Preimplantation genetic diagnosis increases the implantation rate in human in vitro fertilization by avoiding the transfer of chromosomally abnormal embryos. Fertil Steril, 68:1128-1131.

[4] Knight, S.J., Flint, J., 2000. Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis. J Med Genet, 37:401-409.

[5] Munné, S., Fung, J., Cassel, M.J., Marquez, C., Weier, H.U., 1998a. Preimplantation genetic analysis of translocations: case(specific probes for interphase cell analysis. Hum Genet, 102:663-674.

[6] Munné, S., Márquez, C., Reing, A., Garrisi, J., Alikani, M., 1998b. Chromosome abnormalities in embryos obtained after conventional in vitro fertilization and intracytoplasmic sperm injection. Fertil Steril, 69:904-908.

[7] Simpson, J.L., 2001. Changing indications for preimplantation genetic diagnosis (PGD). Molecular and Cellular Endocrinology, 183:S69-S75.

[8] Staessen, C., Tournaye, H., Van Assche, E., Michiels, A., Van Landuyt, L., Devroey, P., Liebaers, I., Van Steirteghem, A., 2003. PGD in 47, XXY Klinefelter’s syndrome patients. Hum Reprod Update, 9:319-330.

[9] Verlinsky, Y., Kuliev, A., 1996. Preimplantation diagnosis of common aneuploidies in infertile couples of advanced maternal age. Hum Reprod, 11:2076-2077.

[10] Wilton, L., 2002. Preimplantation genetic diagnosis for aneuploid screening in early human embryos: a review. Prenat Diagn, 22:512-518.