Crippa A, et al. First meiosis errors in immature oocytes generated by stimulated cycles. Fertil Steril 2006; 86:629.72 72. Amato P, Tashibana M, Sparman M, et al. Three‐patient in vitro fertilization: gene replacement for the prevention of inherited mitochondrial diseases. Fert Steril 2014; 101:31.
73 73. Rechitsky S, Pomerantseva K, Pakhalchuk T, et al. First systematic experience of preimplantation genetic diagnosis for de novo mutations. Reprod BioMed Online 2011; 22:350.
74 74. Verlinsky Y, Rechitsky S, Verlinsky O, et al. Preimplantation diagnosis for p53 tumor suppressor gene mutations. Reprod Bio Med Online 2001; 2:102.
75 75. Verlinsky Y, Rechitsky S, Verlinsky O, et al. Preimplantation diagnosis for sonic hedgehog mutation causing familial holoprosencephaly. N Engl J Med 2003; 348:1449.
76 76. Verlinsky Y, Rechitsky S, Schoolcraft, et al. Preimplantation diagnosis for homeobox gene HLXB9 mutation causing Currarino syndrome. Am J Med Genet 2005; 134A:103.
77 77. He J, McDermont DA, Song Y, et al. Preimplantation genetic diagnosis of human congenital heart disease and Holt–Oram syndrome. Am J Med Genet 2003; 126A:93.
78 78. Kuliev A, Pomerantseva E, Polling D, et al. PGD for inherited cardiac diseases. Reprod Bio Med Online 2012; 24:443
79 79. Verlinsky Y, Rechitsky S, Sharapova T, et al. Preimplantation HLA typing. JAMA 2004; 291:2079.
80 80. Edwards RG. Ethics of PGD: thoughts on the consequences of typing HLA in embryos. Reprod Bio Med Online 2004 9:222.
81 81. Rechitsky S, Kuliev A, Tur‐Kaspa I, et al. Preimplantation HLA typing with preimplantation genetic diagnosis. Reprod Bio Med Online 2004; 6:488.
82 82. vande Velde H, Georgiou I, de Rycke M, et al. Novel universal approach for preimplantation genetic diagnosis of β‐thalassemia in combination with HLA matching of embryos. Hum Reprod 2004; 19:700.
83 83. Kahraman S, Karlilaya G, Sertyel S, et al. Clinical aspects of preimplantation genetic diagnosis of single gene disorders combined with HLA typing. Reprod BioMed Online 2004; 9:529.
84 84. Kuliev A, Rechitsky S, Verlinsky O, et al. Preimplantation diagnosis and HLA typing for hemoglobin disorders. Reprod BioMed Online 2005; 11:362.
85 85. Rechitsky S, Kuliev A, Sharapova T, et al. Preimplantation HLA typing with aneuploidy testing. Reprod BioMed Online 2006; 12:81.
86 86. Kuliev A, Rechitsky S, Tur‐Kaspa I, et al. Preimplantation genetics: improving access to stem cell therapy. Ann NY Acad Sci 2005; 1054:223.
87 87. Chen SU, Su YN, Fang MY, et al. PGD of beta‐thalassaemia and HLA haplotypes using OmniPlex whole genome amplification. Reprod Biomed Online 2008; 17:699.
88 88. Verlinsky Y, Rechitsky S, Sharapova T, et al. Preimplantation diagnosis for immunodeficiencies. Reprod Biomed Online 2007; 14:214–223.
89 89. Reichenbach J, van de Velde H, de Rycke M, et al. First successful bone marrow transplantation for X‐linked chronic granulomatous disease by using preimplantation female gender typing and HLA matching. Pediatrics 2008; 122:e778.
90 90. Goussetis E, Kokkali G, Petrakou E, et al. Successful hematopoietic stem cell transplantation in 2 children with X‐linked chronic granulomatous disease from their unaffected HLA‐identical siblings selected using preimplantation genetic diagnosis combined with HLA typing. Biol Blood Marrow Transplant 2010; 16:344.
91 91. Kuliev A, Packalchuk T, Verlinsky O, et al. Preimplantation diagnosis: efficient tool for human leukocyte antigen matched bone marrow transplantation for thalassemia. Thalassemia Rep 2011; 1:e1.
92 92. Kuliev A, Rechitsky S, Verlinsky O. Atlas of preimplantation genetic diagnosis, 3rd edn. London: CRS Press, Taylor and Francis, 2014.
93 93. Kahraman S, Beyazyurek C, Ekmeksi C, et al. Seven year experience of preimplantation HLA typing: a clinical experience of 327 cycles. Reprod Biomed Online 2011; 23:363.
94 94. Umay KB, Gavaz M, Kumtepe ÇY, et al. Successful hemapoietic stem cell transplantation in 62 children from healthy siblings conceived from preimplantation HLA Matching: a clinical experience of 327 cycles. Reprod Biomed Online 2019; 39(Suppl 1):e13.
95 95. Plachot M. Chromosomal abnormalities in oocytes. Mol Cell Endocrinol 2001; 183:S59.
96 96. Martin RH, Spriggs E, Rademaker AW. Multicolour fluorescence in situ hybridization analysis of aneuploidy and diploidy frequencies in 225,846 sperm from ten normal men. Biol Reprod 1996; 54:394.
97 97. Gropp A. Chromosomal animal model of human disease: fetal trisomy and development failure. In: Berry L, Poswillo DE, eds. Teratology. Berlin: Springer‐Verlag, 1975:17.
98 98. Epstein CJ. Mouse monosomies and trisomies as experimental systems for studying mammalian aneuploidy. Trends Genet 1985; 1:129.
99 99. Dyban A, De Sutter P, Verlinsky Y. Preimplantation cytogenetic analysis. In: Verlinsky Y, Kuliev AM, eds. Preimplantation diagnosis of genetic diseases: a new technique in assisted reproduction. New York: Wiley‐Liss, 1993:93.
100 100. De Sutter P, Dozortsev D, Cieslak J, et al. Parthenogenetic activation of human oocytes by puromycin. J Assist Reprod Genet 1992; 9:328.
101 101. Dyban AP, de Sutter P, Dozortsev D, et al. Visualization of second polar body chromosomes in fertilized and artificially activated mouse oocytes treated with okadaic acid. J Assist Reprod Genet 1992; 9:572.
102 102. Verlinsky Y, Dozortsev D, Evsikov S. Visualization and cytogenetic analysis of second polar body chromosomes following its fusion with one‐cell mouse embryo. J Assist Reprod Genet 1994; 11:123.
103 103. Antonarakis SE, Petersen MB, McInnis MG, et al. The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms. Am J Hum Genet 1992; 50:544.
104 104. Rodman TC. Chromosomes of the first polar body in mammalian meiosis. Exp Cell Res 1971; 68:205.
105 105. Dyban A, de Sutter P, Verlinsky Y. Okadaic acid induces premature chromosome condensation reflecting the cell cycle progression in one cell stage mouse embryos. Mol Reprod Dev 1993; 34:403.
106 106. Tanaka A, Nagayoshi M, Awata S, et al. Preimplantation diagnosis of repeated miscarriage due to chromosomal translocations using metaphase chromosomes of a blastomere biopsied from 4–6 cell stage embryo. Fertil Steril 2004; 81:30.
107 107. Dyban A, Fredine M, Severova E, et al. Detection of aneuploidy in human oocytes and corresponding first polar bodies by FISH. J Assist Reprod Genet 1995; 13:72.
108 108. Munné S, Dailey T, Sultan KM, et al. The use of first polar bodies for preimplantation diagnosis of aneuploidy. Hum Reprod 1995; 10:1014.
109 109. Verlinsky Y, Cieslak J, Freidine M, et al. Polar body diagnosis of common aneuploidies by FISH. J Assist Reprod Genet 1996; 13:157.
110 110. Verlinsky Y, Cieslak J, Ivakhnenko V, et al. Birth of healthy children following preimplantation diagnosis of common aneuploidies by polar FISH analysis. Fertil Steril 1996; 66:126.
111 111. Kuliev A, Cieslak J, Illkewitch Y, et al. Chromosomal abnormalities in a series of 6733 human oocytes in preimplantation diagnosis of age‐related aneuploidies. Reprod Biomed Online 2003 6:54.
112 112. Kuliev A, Cieslak J, Verlinsky Y. Frequency and distribution
