M. Gordillo Et Al. , "The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity," HUMAN MOLECULAR GENETICS , vol.17, no.14, pp.2172-2180, 2008
Gordillo, M. Et Al. 2008. The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity. HUMAN MOLECULAR GENETICS , vol.17, no.14 , 2172-2180.
Gordillo, M., Vega, H., Trainer, A. H., Hou, F., Sakai, N., Luque, R., ... Kayserili, H.(2008). The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity. HUMAN MOLECULAR GENETICS , vol.17, no.14, 2172-2180.
Gordillo, Miriam Et Al. "The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity," HUMAN MOLECULAR GENETICS , vol.17, no.14, 2172-2180, 2008
Gordillo, Miriam Et Al. "The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity." HUMAN MOLECULAR GENETICS , vol.17, no.14, pp.2172-2180, 2008
Gordillo, M. Et Al. (2008) . "The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity." HUMAN MOLECULAR GENETICS , vol.17, no.14, pp.2172-2180.
@article{article, author={Miriam Gordillo Et Al. }, title={The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity}, journal={HUMAN MOLECULAR GENETICS}, year=2008, pages={2172-2180} }