참고문헌
- French FE, Bierman JM. Probabilities of fetal mortality. Publ Hlth Rep 1967; 77: 835-47
- Dejmek J, Vojtassak J, Malova J. Cytogenetic analysis of 1508 spontaneous abortions originating from south Slovakia. Eur J Obstet Gynecol Reprod Bioi 1992; 46: 129-36 https://doi.org/10.1016/0028-2243(92)90257-Y
- Boue A, Boue J, Gropp A. Cytogenetics in pregnancy wastage. In; Harris H, Hirschhorn K, editors. Advances in human genetics. New York: Plenum Press; 1985. p.1-57
- Carp HJA, Toder V, Maschiach S, Nebel L, Serr DM. Recurrent miscarriage: A review of current concepts, immune mechanisms and result of treatment. Obstet Gynecol Survey 1990; 45: 657-69 https://doi.org/10.1097/00006254-199010000-00003
- Daya S, Clark DA. Alloimmunity. In; Gleicher N. Principles and practice of medical therapy in pregnancy. Norwalk, Connecticut: Appleton & Lange; 1992. p.407-13.
- Glass RH, Globus MS. Habitual abortion. Fertil Steril 1978; 29: 257-65
- Penrose LS, Delhanty JD. Triploid cell cultures from a macerated foetus. Lancet 1961;1: 1261-2
- Ward BE, Henry GP, Robinson A. Cytogenetic studies in 100 couples with recurrent spontaneous abortions. Am J Hum Genet 1980; 32: 549-54
- Stenchever MA, Park KJ, Daines TL, Allen MA, Stenchever MR. Cytogenetics of habitual abortion and other reproductive wastage. Am J Obstet GynecoI 1977; 127: 143-50
- Mameli M, Cardia S, Milia A, Aste A, Santucci S, Genazzani AR. Cytogenetic study in 50 couples with recurrent abortions. Gynecol Obstet Invest 1984; 17: 84-8 https://doi.org/10.1159/000299127
- Portnoi MF, Joye N, Van den Akker J, Morlier G, Taillemite JL. Karyotypes of 1142 couples with recurrent abortion. Obstet Gynecol 1988; 72: 31-4.
- Makino S, Tabuchi T, Nakada K, Iwasaki K, Tamura S, Iizuka R. Chromosomal analysis in Japanese couples with repeated spontaneous abortions. Int J Fertil 1990; 35: 266-70
- Fryns JP, Van Buggenhout G. Structural chromosome rearrangements in couples with recurrent fetal wastage. Eur J Obstet Gynecol Reprod BioI 1998; 81: 171-6 https://doi.org/10.1016/S0301-2115(98)00185-7
- 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: 117-9
- Evans JA, Canning N, Hunter AGW, Martsolf IT, Ray M, Hamerton JL, et al. A cytogenetic survey of 14069 newborn infants: An analysis of the signifi-cance and cytologic behavior of the Robertsonian and reciprocal translocations. Cytogenet Cell Genet 1978; 20: 96-123 https://doi.org/10.1159/000130843
- Nielsen J, Hansen KB, Sillesen I, Videbech P. Chromosome abnormalities in newborn children. Physical aspects. Hum Genet 1981; 59: 194-200
- Court Brown WM. Human population cytogenetics. Amsterdam: North-Holland; 1967. p.25
- Nielsen J, Rasmussen K. Autosomal reciprocal translocations and 13/14 translocations: a populations study. Clin Genet 1976; 10: 161-77 https://doi.org/10.1111/j.1399-0004.1976.tb00029.x
- Fryns JP, Kleczkowska A, Kubien E, Van den Berghe H. Structural chromosome rearrangements in couples with repeated miscarriages. Experience in Leuvan. J Genet Hum. 1988; 36: 59-61
- Davis JR, Weinstein L, Veomett IC, Shenker L, Giles HR, Hauck L. Balanced translocation karyotypes in patients with repetitive abortion. Am J Obstet Gynecol 1982; 144: 229-33
- Antonio P, Carmen R, Francesca V, Yolanda M, Carles G, Jose E, et al. In vitro fertilization plus preimplantation genetic diagnosis in patients with recurrent miscarriage: an analysis of chromosome abnormalities in human preimplantation embryos. Fertil Steril 1999; 71: 1033-9 https://doi.org/10.1016/S0015-0282(99)00143-0
- Fryns JP, Kleczkowska A, Van den Berghe H. Paracentric inversions in man. Hum Genet 1986; 73: 205-13 https://doi.org/10.1007/BF00401228
- Nielsen J, Stillesen I. Incidence of chromosome aberrations among 11148 newborn children. Hum Genet 1975; 30: 1-12 https://doi.org/10.1007/BF00273626
- Fryns JP, Kleczkowska A, Van den Berghe H. Pericentric inversion in man. Hum Genet 1987; 75: 333-8 https://doi.org/10.1007/BF00284103
- Teo SH, Tan M, Knight L, Yeo SH, Ng I. Pericentric inversion 9: incidence and clinical significance. Ann Acad Moo Singapore 1995; 24: 302-4
- Turleau C, Chavin CF, de Grouchy 1. Cytogenetic investigation in 413 couples with spontaneous abortions. Eur J Obstet Gynecol Repro BioI 1979; 9: 65-74 https://doi.org/10.1016/0028-2243(79)90001-7
- Davalos IP, Rivas F, Ramos AL, Galaviz C, Sandoval L, Rivera H. Inv(9)(p24q13) in three sterile brothers. Ann Genet 2000; 43: 51-4 https://doi.org/10.1016/S0003-3995(00)00013-7
- Vermeulen SJ, Speleman F, Vanransbeeck L, Verspeet J, Menten B, Verschraegen-Spae MR, et al. Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del (18p) recombinant chromosome. Eur J Hum Genet. 2005; 13: 52-8. https://doi.org/10.1038/sj.ejhg.5201281