M. B. Mutlu Et Al. , "A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus," EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.59, no.11, pp.604-606, 2016
Mutlu, M. B. Et Al. 2016. A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.59, no.11 , 604-606.
Mutlu, M. B., Cetinkaya, A., Koc, N., Ceylaner, G., Erguner, B., Aydin, H., ... Karaman, S.(2016). A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.59, no.11, 604-606.
Mutlu, Mehmet Et Al. "A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus," EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.59, no.11, 604-606, 2016
Mutlu, Mehmet B. Et Al. "A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.59, no.11, pp.604-606, 2016
Mutlu, M. B. Et Al. (2016) . "A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.59, no.11, pp.604-606.
@article{article, author={Mehmet Burak Mutlu Et Al. }, title={A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus}, journal={EUROPEAN JOURNAL OF MEDICAL GENETICS}, year=2016, pages={604-606} }