Twigg, S. R. F. Et Al. 2012. Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization. AMERICAN JOURNAL OF HUMAN GENETICS , vol.91, no.5 , 897-905.

Twigg, S. R. F., Lloyd, D., Jenkins, D., Elcioglu, N. E., Cooper, C. D. O., Al-Sannaa, N., ... Annagur, A.(2012). Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization. AMERICAN JOURNAL OF HUMAN GENETICS , vol.91, no.5, 897-905.

Twigg, Stephen Et Al. "Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization," AMERICAN JOURNAL OF HUMAN GENETICS , vol.91, no.5, 897-905, 2012

Twigg, Stephen R. Et Al. "Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization." AMERICAN JOURNAL OF HUMAN GENETICS , vol.91, no.5, pp.897-905, 2012

Twigg, S. R. F. Et Al. (2012) . "Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization." AMERICAN JOURNAL OF HUMAN GENETICS , vol.91, no.5, pp.897-905.

@article{article, author={Stephen R. F. Twigg Et Al. }, title={Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2012, pages={897-905} }