Publications
Found 1 results
Filters: Author is S. Kalkanlı-Taş [Clear All Filters]
“Chromosome heteromorphisms are more frequent in couples with recurrent abortions”, vol. 11, pp. 3847-3851, 2012.
,
Blumberg BD, Shulkin JD, Rotter JI, Mohandas T, et al. (1982). Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion. Am. J. Hum. Genet. 34: 948-960.
PMid:7180849 PMCid:1685697
Brothman AR, Schneider NR, Saikevych I, Cooley LD, et al. (2006). Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for years. Arch. Pathol. Lab. Med. 130: 947-949.
PMid:16831047
Caglayan AO, Ozyazgan I, Demiryilmaz F and Ozgun MT (2010). Are heterochromatin polymorphisms associated with recurrent miscarriage? J. Obstet. Gynaecol. Res. 36: 774-776.
http://dx.doi.org/10.1111/j.1447-0756.2010.01207.x
PMid:20666944
Codina-Pascual M, Navarro J, Oliver-Bonet M, Kraus J, et al. (2006). Behaviour of human heterochromatic regions during the synapsis of homologous chromosomes. Hum. Reprod. 21: 1490-1497.
http://dx.doi.org/10.1093/humrep/del028
PMid:16484310
De la Fuente-Cortés BE, Cerda-Flores RM, Davila-Rodriguez MI, Garcia-Vielma C, et al. (2009). Chromosomal abnormalities and polymorphic variants in couples with repeated miscarriage in Mexico. Reprod. Biomed. Online 18: 543-548.
http://dx.doi.org/10.1016/S1472-6483(10)60132-0
de Braekleer M and Dao TN (1990). Cytogenetic studies in couples experiencing repeated pregnancy losses. Hum. Reprod. 5: 519-528.
Düzcan F, Atmaca M, Cetin GO and Bagci H (2003). Cytogenetic studies in patients with reproductive failure. Acta Obstet. Gynecol. Scand. 82: 53-56.
PMid:12580840
Eiben B, Leipoldt M, Rammelsberg O, Krause W, et al. (1987). High incidence of minor chromosomal variants in teratozoospermic males. Andrologia 19: 684-687.
http://dx.doi.org/10.1111/j.1439-0272.1987.tb01929.x
PMid:3434859
Karpen G and Kndow S (1998). Meiosis: Chromosome Bhaviour and Spindle Dynamics. In: Froniiers in Biology (Endow S and Glover D, eds.). Oxford University Press, Oxford. 203-247.
Madon PF, Athalye AS and Parikh FR (2005). Polymorphic variants on chromosomes probably play a significant role in infertility. Reprod. Biomed. Online 11: 726-732.
http://dx.doi.org/10.1016/S1472-6483(10)61691-4
Makino T, Tabuchi T, Nakada K, Iwasaki K, et al. (1990). Chromosomal analysis in Japanese couples with repeated spontaneous abortions. Int. J. Fertil. 35: 266-270.
PMid:1980661
Mau UA, Backert IT, Kaiser P and Kiesel L (1997). Chromosomal findings in 150 couples referred for genetic counselling prior to intracytoplasmic sperm injection. Hum. Reprod. 12: 930-937.
http://dx.doi.org/10.1093/humrep/12.5.930
PMid:9194642
Nakamura Y, Kitamura M, Nishimura K, Koga M, et al. (2001). Chromosomal variants among 1790 infertile men. Int. J. Urol. 8: 49-52.
http://dx.doi.org/10.1046/j.1442-2042.2001.00242.x
PMid:11240825
Penna-Videau S, Araujo H, Ballesta F, Ballesca JL, et al. (2001). Chromosomal abnormalities and polymorphisms in infertile men. Arch. Androl. 46: 205-210.
http://dx.doi.org/10.1080/01485010151096504
PMid:11339646
Sahin FI, Yilmaz Z, Yuregir OO, Bulakbasi T, et al. (2008). Chromosome heteromorphisms: an impact on infertility. J. Assist. Reprod. Genet. 25: 191-195.
http://dx.doi.org/10.1007/s10815-008-9216-3
PMid:18461436 PMCid:2582066
Verma R and Babu A (1989). Human Chromosomes Manual of Basic Techniques. Pergamon Press, New York.
Wyandt HE and Tonk VS (2004). Atlas of Human Chromosome Heteromorphisms. Kluwer, Dordrecht.
Yakin K, Balaban B and Urman B (2005). Is there a possible correlation between chromosomal variants and spermatogenesis? Int. J. Urol. 12: 984-989.
http://dx.doi.org/10.1111/j.1442-2042.2005.01185.x
PMid:16351655