Altıok Clark, Ö. Et Al. 2017. A de novo ins(21;13) and two interstitial deletions in 13q in a boy with multple congenital anomalies. MOLECULAR CYTOGENETICS , vol.10 .

Altıok Clark, Ö., Cetin, G. O., Nur, B., Toylu, A., Karaüzüm, S., & Mıhçı, E., (2017). A de novo ins(21;13) and two interstitial deletions in 13q in a boy with multple congenital anomalies. MOLECULAR CYTOGENETICS , vol.10.

Altıok Clark, ÖZDEN Et Al. "A de novo ins(21;13) and two interstitial deletions in 13q in a boy with multple congenital anomalies," MOLECULAR CYTOGENETICS , vol.10, 2017

Altıok Clark, ÖZDEN A. Et Al. "A de novo ins(21;13) and two interstitial deletions in 13q in a boy with multple congenital anomalies." MOLECULAR CYTOGENETICS , vol.10, 2017

Altıok Clark, Ö. Et Al. (2017) . "A de novo ins(21;13) and two interstitial deletions in 13q in a boy with multple congenital anomalies." MOLECULAR CYTOGENETICS , vol.10.

@article{article, author={ÖZDEN ALTIOK CLARK Et Al. }, title={A de novo ins(21;13) and two interstitial deletions in 13q in a boy with multple congenital anomalies}, journal={MOLECULAR CYTOGENETICS}, year=2017}