ÇAĞLAYAN, A. O. Et Al. 2017. ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features. COLD SPRING HARBOR MOLECULAR CASE STUDIES , vol.3, no.5 .

ÇAĞLAYAN, A. O., Sezer, R. G., Kaymakcalan, H., Ulgen, E., Yavuz, T., Baranoski, J. F., ... Bozaykut, A.(2017). ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features. COLD SPRING HARBOR MOLECULAR CASE STUDIES , vol.3, no.5.

ÇAĞLAYAN, AHMET Et Al. "ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features," COLD SPRING HARBOR MOLECULAR CASE STUDIES , vol.3, no.5, 2017

ÇAĞLAYAN, AHMET O. Et Al. "ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features." COLD SPRING HARBOR MOLECULAR CASE STUDIES , vol.3, no.5, 2017

ÇAĞLAYAN, A. O. Et Al. (2017) . "ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features." COLD SPRING HARBOR MOLECULAR CASE STUDIES , vol.3, no.5.

@article{article, author={AHMET OKAY ÇAĞLAYAN Et Al. }, title={ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features}, journal={COLD SPRING HARBOR MOLECULAR CASE STUDIES}, year=2017}