Perçin, F. E. Et Al. 2000. A Case of Partial Trisomy 13 Findings with 46,XX,der(7)t(7;13)(p22;q31)mat Karyotype. Turkish Journal Of Medical Sciences , vol.30 , 377-380.

Perçin, F. E., Süngü, Y. S., Ilgın Ruhi, H., Törel Ergür, A., Düzcan, F., & Sezgin, İ., (2000). A Case of Partial Trisomy 13 Findings with 46,XX,der(7)t(7;13)(p22;q31)mat Karyotype. Turkish Journal Of Medical Sciences , vol.30, 377-380.

Perçin, FERDA Et Al. "A Case of Partial Trisomy 13 Findings with 46,XX,der(7)t(7;13)(p22;q31)mat Karyotype," Turkish Journal Of Medical Sciences , vol.30, 377-380, 2000

Perçin, FERDA E. Et Al. "A Case of Partial Trisomy 13 Findings with 46,XX,der(7)t(7;13)(p22;q31)mat Karyotype." Turkish Journal Of Medical Sciences , vol.30, pp.377-380, 2000

Perçin, F. E. Et Al. (2000) . "A Case of Partial Trisomy 13 Findings with 46,XX,der(7)t(7;13)(p22;q31)mat Karyotype." Turkish Journal Of Medical Sciences , vol.30, pp.377-380.

@article{article, author={FERDA EMRİYE PERÇİN Et Al. }, title={A Case of Partial Trisomy 13 Findings with 46,XX,der(7)t(7;13)(p22;q31)mat Karyotype}, journal={Turkish Journal Of Medical Sciences}, year=2000, pages={377-380} }