Sayar, C. Et Al. 2007. A prenatal case of a 46,XX[44]/ 48,XX,+2XMAR[11].ish(D14Z1/ D22Z1+,WCP+)mat. karyotype, with marker chromosome effects on the phenotypes in three generations. CHROMOSOME RESEARCH , vol.15, no.1 , 122.

Sayar, C., Toksoy, G., Türköver, B., Yardımcı, T., & Şahinoğlu, Z., (2007). A prenatal case of a 46,XX[44]/ 48,XX,+2XMAR[11].ish(D14Z1/ D22Z1+,WCP+)mat. karyotype, with marker chromosome effects on the phenotypes in three generations. CHROMOSOME RESEARCH , vol.15, no.1, 122.

Sayar, Ceyhan Et Al. "A prenatal case of a 46,XX[44]/ 48,XX,+2XMAR[11].ish(D14Z1/ D22Z1+,WCP+)mat. karyotype, with marker chromosome effects on the phenotypes in three generations," CHROMOSOME RESEARCH , vol.15, no.1, 122, 2007

Sayar, Ceyhan Et Al. "A prenatal case of a 46,XX[44]/ 48,XX,+2XMAR[11].ish(D14Z1/ D22Z1+,WCP+)mat. karyotype, with marker chromosome effects on the phenotypes in three generations." CHROMOSOME RESEARCH , vol.15, no.1, pp.122, 2007

Sayar, C. Et Al. (2007) . "A prenatal case of a 46,XX[44]/ 48,XX,+2XMAR[11].ish(D14Z1/ D22Z1+,WCP+)mat. karyotype, with marker chromosome effects on the phenotypes in three generations." CHROMOSOME RESEARCH , vol.15, no.1, p.122.

@article{article, author={Ceyhan Sayar Et Al. }, title={A prenatal case of a 46,XX[44]/ 48,XX,+2XMAR[11].ish(D14Z1/ D22Z1+,WCP+)mat. karyotype, with marker chromosome effects on the phenotypes in three generations}, journal={CHROMOSOME RESEARCH}, year=2007, pages={122} }