D. Doherty Et Al. , "Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)," JOURNAL OF MEDICAL GENETICS , vol.47, no.1, pp.8-21, 2010
Doherty, D. Et Al. 2010. Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis). JOURNAL OF MEDICAL GENETICS , vol.47, no.1 , 8-21.
Doherty, D., Parisi, M. A., Finn, L. S., Gunay-Aygun, M., Al-Mateen, M., Bates, D., ... Clericuzio, C.(2010). Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis). JOURNAL OF MEDICAL GENETICS , vol.47, no.1, 8-21.
Doherty, D. Et Al. "Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)," JOURNAL OF MEDICAL GENETICS , vol.47, no.1, 8-21, 2010
Doherty, D. Et Al. "Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)." JOURNAL OF MEDICAL GENETICS , vol.47, no.1, pp.8-21, 2010
Doherty, D. Et Al. (2010) . "Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)." JOURNAL OF MEDICAL GENETICS , vol.47, no.1, pp.8-21.
@article{article, author={D. Doherty Et Al. }, title={Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)}, journal={JOURNAL OF MEDICAL GENETICS}, year=2010, pages={8-21} }