Caglayan, A. O. Et Al. 2013. Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum. CLINICAL GENETICS , vol.84, no.4 , 394-395.

Caglayan, A. O., PER, H., Akgumus, G., GÜMÜŞ, H., Baranoski, J., CANPOLAT, M., ... CALIK, M.(2013). Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum. CLINICAL GENETICS , vol.84, no.4, 394-395.

Caglayan, A. Et Al. "Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum," CLINICAL GENETICS , vol.84, no.4, 394-395, 2013

Caglayan, A. O. Et Al. "Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum." CLINICAL GENETICS , vol.84, no.4, pp.394-395, 2013

Caglayan, A. O. Et Al. (2013) . "Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum." CLINICAL GENETICS , vol.84, no.4, pp.394-395.

@article{article, author={A. O. Caglayan Et Al. }, title={Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum}, journal={CLINICAL GENETICS}, year=2013, pages={394-395} }