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2012
H. Akbas, İsi, H., İsi, H., Oral, D., Turkyılmaz, A., Kalkanlı-Taş, S., Simsek, S., Balkan, M., Sakar, M. N., Fidanboy, M., Alp, M. N., and Budak, T., 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
2010
M. Balkan, Akbas, H., İsi, H., İsi, H., Oral, D., Turkyılmaz, A., Kalkanli, S., Simsek, S., Fidanboy, M., Alp, M. N., Gedik, A., and Budak, T., Cytogenetic analysis of 4216 patients referred for suspected chromosomal abnormalities in Southeast Turkey, vol. 9, pp. 1094-1103, 2010.
Akgül M, Ozkinay F, Ercal D, Cogulu O, et al. (2009). Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: report and review. J. Assist. Reprod. Genet. 26: 119-122. http://dx.doi.org/10.1007/s10815-009-9296-8 PMid:19184395 PMCid:2654936   Al Husain M and Zaki OK (1999). A survey of 1,000 cases referred for cytogenetic study to King Khalid University Hospital, Saudi Arabia. Hum. Hered. 49: 208-214. http://dx.doi.org/10.1159/000022877 PMid:10436383   Amudha S, Aruna N and Rajangam S (2005). Consanguinity and chromosomal abnormality. Indian J. Hum. Genet. 11: 108-110. http://dx.doi.org/10.4103/0971-6866.16812   Awwad R, Veach PM, Bartels DM and LeRoy BS (2008). Culture and acculturation influences on Palestinian perceptions of prenatal genetic counseling. J. Genet. Couns. 17: 101-116. http://dx.doi.org/10.1007/s10897-007-9131-2 PMid:17963027   Balkan M, Tekes S and Gedik A (2008). Cytogenetic and Y chromosome microdeletion screening studies in infertile males with oligozoospermia and azoospermia in Southeast Turkey. J. Assist. Reprod. Genet. 25: 559-565. http://dx.doi.org/10.1007/s10815-008-9272-8 PMid:18953646 PMCid:2593766   Butler MG and Hamill T (1995). Blood specimens from patients referred for cytogenetic analysis: Vanderbilt University experience from 1985 to 1992. South Med. J. 88: 309-314. http://dx.doi.org/10.1097/00007611-199503000-00012 PMid:7886528   Chandley AC (1990). Infertility and Recurrent Abortions. In: Principles and Practice of Medical Genetics (Emery A and Rimoin D, eds.). Chapter 21. Churchill Livingstone, New York, 313-319.   Duarte AC, Cunha E, Roth JM, Ferreira FL, et al. (2004). Cytogenetics of genetic counseling patients in Pelotas, Rio Grande do Sul, Brazil. Genet. Mol. Res. 3: 303-308. PMid:15614723   Düzcan F, Atmaca M, Cetin GO and Bagci H (2003). Cytogenetic studies in patients with reproductive failure. Acta Obstet. Gynecol. 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An International System for Human Cytogenetic Nomenclature. Recommendations of the International Standing Committee on Human Cytogenetic Nomenclature (Mitelman F, ed.). S. Karger Publishers Inc., Basel.   Kim SS, Jung SC, Kim HJ, Moon HR, et al. (1999). Chromosome abnormalities in a referred population for suspected chromosomal aberrations: a report of 4117 cases. J. Korean Med. Sci. 14: 373-376. PMid:10485615 PMCid:3054395   Méhes K and Bajnoczky K (1981). Incidence of major chromosomal abnormalities. Clin. Genet. 19: 75-76. http://dx.doi.org/10.1111/j.1399-0004.1981.tb00672.x PMid:7460384   Milia A, Cardia S, Aste A, Santucci S, et al. (1984). Cytogenetic study on 282 patients with suspected chromosomal aberration. Eur. J. Obstet. Gynecol. Reprod. Biol. 18: 207-210. http://dx.doi.org/10.1016/0028-2243(84)90118-7   Patil SR, Lubs HA, Brown J, Cohen M, et al. (1977). Incidence of major chromosome abnormalities in children. Cytogenet. Cell Genet. 18: 3102-3106. http://dx.doi.org/10.1159/000130774 PMid:880833   Salamanca F and Armendares S (1974). C bands in human metaphase chromosomes treated by barium hydroxide. Ann. Genet. 17: 135-136. PMid:4139928   Samonte RV, Conte RA, Ramesh KH and Verma RS (1996). Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9. Hum. Genet. 98: 576-580. http://dx.doi.org/10.1007/s004390050262 PMid:8882878   Santos CB, Boy RT, Santos JM, Silva MPS, et al. (2000). Chromosomal investigations in patients with mental retardation and/or congenital malformations. Genet. Mol. Biol. 23: 703-707. http://dx.doi.org/10.1590/S1415-47572000000400002   Seabright M (1971). A rapid banding technique for human chromosomes. Lancet 2: 971-972. http://dx.doi.org/10.1016/S0140-6736(71)90287-X   Solak M, Fistik T, Eser B, Söylemez Z, et al. (2007). Cytogenetic Analyses in Medical Genetic Laboratory of Medical Biology Department in Afyonkarahisar Kocatepe University. Osmangazi J. Med. 29: 93-99.   Sumner AT (1972). A simple technique for demonstrating centromeric heterochromatin. Exp. Cell Res. 75: 304-306. http://dx.doi.org/10.1016/0014-4827(72)90558-7   Taylor AI (1968). Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome. J. Med. Genet. 5: 227-252. http://dx.doi.org/10.1136/jmg.5.3.227 PMid:5708029 PMCid:1468648   Tunç E, Demirhan O, Demir C and Tastemir D (2007). Cytogenetic study of recurrent miscarriages and their parents. Genetika 43: 545-552. PMid:17555132   Verma RS and Dosik H (1980). Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: a report of 357 cases. Clin. Genet. 17: 305-308. http://dx.doi.org/10.1111/j.1399-0004.1980.tb00154.x PMid:7438487   Yuce H, Tekedereli I and Elyas H (2007). Cytogenetic results of recurrent spontaneous abortions in Turkey. Med. Sci. Monit. 13: CR286-CR289. PMid:17534236