E. Erdal Et Al. , "Mutation analysis of the Vangl2 coding region revealed no common cause for tetralogy of Fallot," JOURNAL OF INTERNATIONAL MEDICAL RESEARCH , vol.35, no.6, pp.867-872, 2007
Erdal, E. Et Al. 2007. Mutation analysis of the Vangl2 coding region revealed no common cause for tetralogy of Fallot. JOURNAL OF INTERNATIONAL MEDICAL RESEARCH , vol.35, no.6 , 867-872.
Erdal, E., Erdal, C., Bulut, G., Kunter, I., Kir, M., Atabey, N., ... Acikel, U.(2007). Mutation analysis of the Vangl2 coding region revealed no common cause for tetralogy of Fallot. JOURNAL OF INTERNATIONAL MEDICAL RESEARCH , vol.35, no.6, 867-872.
Erdal, ŞERİFE Et Al. "Mutation analysis of the Vangl2 coding region revealed no common cause for tetralogy of Fallot," JOURNAL OF INTERNATIONAL MEDICAL RESEARCH , vol.35, no.6, 867-872, 2007
Erdal, ŞERİFE E. Et Al. "Mutation analysis of the Vangl2 coding region revealed no common cause for tetralogy of Fallot." JOURNAL OF INTERNATIONAL MEDICAL RESEARCH , vol.35, no.6, pp.867-872, 2007
Erdal, E. Et Al. (2007) . "Mutation analysis of the Vangl2 coding region revealed no common cause for tetralogy of Fallot." JOURNAL OF INTERNATIONAL MEDICAL RESEARCH , vol.35, no.6, pp.867-872.
@article{article, author={ŞERİFE ESRA ERDAL BAĞRIYANIK Et Al. }, title={Mutation analysis of the Vangl2 coding region revealed no common cause for tetralogy of Fallot}, journal={JOURNAL OF INTERNATIONAL MEDICAL RESEARCH}, year=2007, pages={867-872} }