1. Hardy K, Martin KL, Leese HJ, Winston RM, Handyside AH. Human preimplantation development in vitro is not adversely affected by biopsy at the 8-cell stage. Hum Reprod 1990;5:708-714.
3. Staessen C, Van Assche E, Joris H, Bonduelle M, Vandervorst M, Liebaers I, Van Steirteghem A. Clinical experience of sex determination by fluorescent in-situ hybridization for preimplantation genetic diagnosis. Mol Hum Reprod 1999;5:382-389.
4. Goossens V, Traeger-Synodinos J, Coonen E, De Rycke M, Moutou C, Pehlivan T, Derks-Smeets IA, Harton G. ESHRE PGD Consortium data collection XI: cycles from January to December 2008 with pregnancy follow-up to October 2009. Hum Reprod 2012;27:1887-1911.
5. de Boer KA, Catt JW, Jansen RP, Leigh D, McArthur S. Moving to blastocyst biopsy for preimplantation genetic diagnosis and single embryo transfer at Sydney IVF. Fertil Steril 2004;82:295-298.
6. Gardner DK, Vella P, Lane M, Wagley L, Schlenker T, Schoolcraft WB. Culture and transfer of human blastocysts increases implantation rates and reduces the need for multiple embryo transfers. Fertil Steril 1998;69:84-88.
7. McArthur SJ, Leigh D, Marshall JT, de Boer KA, Jansen RP. Pregnancies and live births after trophectoderm biopsy and preimplantation genetic testing of human blastocysts. Fertil Steril 2005;84:1628-1636.
8. Schoolcraft WB, Treff NR, Stevens JM, Ferry K, Katz-Jaffe M, Scott RT Jr. Live birth outcome with trophectoderm biopsy, blastocyst vitrification, and single-nucleotide polymorphism microarray-based comprehensive chromosome screening in infertile patients. Fertil Steril 2011;96:638-640.
9. Verlinsky Y, Cieslak J, Ivakhnenko V, Lifchez A, Strom C, Kuliev A. Birth of healthy children after preimplantation diagnosis of common aneuploidies by polar body fluorescent in situ hybridization analysis: Preimplantation Genetics Group. Fertil Steril 1996;66:126-129.
10. Munne S, Sandalinas M, Escudero T, Fung J, Gianaroli L, Co-hen J. Outcome of preimplantation genetic diagnosis of translocations. Fertil Steril 2000;73:1209-1218.
11. Munne S, Sandalinas M, Escudero T, Marquez C, Cohen J. Chromosome mosaicism in cleavage-stage human embryos: evidence of a maternal age effect. Reprod Biomed Online 2002;4:223-232.
12. Fiorentino F, Biricik A, Nuccitelli A, De Palma R, Kahraman S, Iacobelli M, Trengia V, Caserta D, Bonu MA, Borini A, Baldi M. Strategies and clinical outcome of 250 cycles of preimplantation genetic diagnosis for single gene disorders. Hum Reprod 2006;21:670-684.
13. Kim MJ, Lee HS, Choi HW, Lim CK, Cho JW, Kim JY, Song IO, Kang IS. Establishment and application of molecular genetic techniques for preimplantation genetic diagnosis of osteogenesis imperfecta. Korean J Reprod Med 2008;35:99-110.
14. Holding C, Monk M. Diagnosis of beta-thalassaemia by DNA amplification in single blastomeres from mouse preimplantation embryos. Lancet 1989;2:532-535.
15. Lee HS, Choi HW, Lim CK, Min DM, Byun HK, Kim JY, Koong MK, Yoo HW, Kim SC, Jun JH, Kang IS. Successful preimplantation genetic diagnosis for ornithine transcarbamylase deficiency, junctional epidermolysis bullosa and lactic acidosis using duplex nested PCR: delivery of healthy baby by specific preimplantation genetic diagnosis for ornithine tran. Korean J Obstet Gynecol 2004;47:708-718.
16. Dreesen JC, Jacobs LJ, Bras M, Herbergs J, Dumoulin JC, Geraedts JP, Evers JL, Smeets HJ. Multiplex PCR of polymorphic markers flanking the CFTR gene: a general approach for preimplantation genetic diagnosis of cystic fibrosis. Mol Hum Reprod 2000;6:391-396.
19. Telenius H, Carter NP, Bebb CE, Nordenskjold M, Ponder BA, Tunnacliffe A. Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics 1992;13:718-725.
20. Handyside AH, Robinson MD, Simpson RJ, Omar MB, Shaw MA, Grudzinskas JG, Rutherford A. Isothermal whole genome amplification from single and small numbers of cells: a new era for preimplantation genetic diagnosis of inherited disease. Mol Hum Reprod 2004;10:767-772.
21. Burlet P, Frydman N, Gigarel N, Kerbrat V, Tachdjian G, Feyereisen E, Bonnefont JP, Frydman R, Munnich A, Steffann J. Multiple displacement amplification improves PGD for fragile X syndrome. Mol Hum Reprod 2006;12:647-652.
22. Langmore JP. Rubicon Genomics, Inc. Pharmacogenomics 2002;3:557-560.
23. Barker DL, Hansen MS, Faruqi AF, Giannola D, Irsula OR, Lasken RS, Latterich M, Makarov V, Oliphant A, Pinter JH, Shen R, Sleptsova I, Ziehler W, Lai E. Two methods of wholegenome amplification enable accurate genotyping across a 2320-SNP linkage panel. Genome Res 2004;14:901-907.
24. Treff NR, Su J, Kasabwala N, Tao X, Miller KA, Scott RT Jr. Robust embryo identification using first polar body single nucleotide polymorphism microarray-based DNA fingerprinting. Fertil Steril 2010;93:2453-2455.
26. Colls P, Escudero T, Fischer J, Cekleniak NA, Ben-Ozer S, Meyer B, Damien M, Grifo JA, Hershlag A, Munne S. Validation of array comparative genome hybridization for diagnosis of translocations in preimplantation human embryos. Reprod Biomed Online 2012;24:621-629.
28. Wells D, Kaur K, Grifo J, Glassner M, Taylor JC, Fragouli E, Munne S. Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation. J Med Genet 2014;51:553-562.
29. Lukaszuk K, Pukszta S, Wells D, Cybulska C, Liss J, Plociennik L, Kuczynski W, Zabielska J. Routine use of next-generation se-quencing for preimplantation genetic diagnosis of blastomeres obtained from embryos on day 3 in fresh in vitro fertilization cycles. Fertil Steril 2015;103:1031-1036.
30. Fiorentino F, Bono S, Biricik A, Nuccitelli A, Cotroneo E, Cottone G, Kokocinski F, Michel CE, Minasi MG, Greco E. Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cycles. Hum Reprod 2014;29:2802-2813.
31. Handyside AH, Lesko JG, Tarin JJ, Winston RM, Hughes MR. Birth of a normal girl after in vitro fertilization and preimplan-tation diagnostic testing for cystic fibrosis. N Engl J Med 1992;327:905-909.
32. Harper JC, Boelaert K, Geraedts J, Harton G, Kearns WG, Moutou C, Muntjewerff N, Repping S, SenGupta S, Scriven PN, Traeger-Synodinos J, Vesela K, Wilton L, Sermon KD. ESHRE PGD Consortium data collection V: cycles from January to De-cember 2002 with pregnancy follow-up to October 2003. Hum Reprod 2006;21:3-21.
33. Lim CK, Jun JH, Min DM, Lee HS, Kim JY, Koong MK, Kang IS. Efficacy and clinical outcome of preimplantation genetic diagnosis using FISH for couples of reciprocal and Robertsonian translocations: the Korean experience. Prenat Diagn 2004;24:556-561.
34. Kim JY, Lim CK, Song IO, Yoo KJ, Yang KM, Han KS, Hur K, Song JH, Jun JH, Min DM, Park SY, Jun JY, Koong MK, Kang IS. Outcome of preimplantation genetic diagnosis for chromosome aneuploidy and genetic disease. Korean J Fertil Steril 2002;29:269-278.
35. Munne S, Cohen J, Sable D. Preimplantation genetic diagnosis for advanced maternal age and other indications. Fertil Steril 2002;78:234-236.
36. Mastenbroek S, Twisk M, van Echten-Arends J, Sikkema-Raddatz B, Korevaar JC, Verhoeve HR, Vogel NE, Arts EG, de Vries JW, Bossuyt PM, Buys CH, Heineman MJ, Repping S, van der Veen F. In vitro fertilization with preimplantation genetic screening. N Engl J Med 2007;357:9-17.
37. Scott RT Jr, Upham KM, Forman EJ, Hong KH, Scott KL, Taylor D, Tao X, Treff NR. Blastocyst biopsy with comprehensive chromosome screening and fresh embryo transfer significantly increases in vitro fertilization implantation and delivery rates: a randomized controlled trial. Fertil Steril 2013;100:697-703.
38. Rechitsky S, Verlinsky O, Chistokhina A, Sharapova T, Ozen S, Masciangelo C, Kuliev A, Verlinsky Y. Preimplantation genetic diagnosis for cancer predisposition. Reprod Biomed Online 2002;5:148-155.
39. Kahraman S, Beyazyurek C, Ekmekci CG. Seven years of experience of preimplantation HLA typing: a clinical overview of 327 cycles. Reprod Biomed Online 2011;23:363-371.