E. A. Otto Et Al. , "Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)," JOURNAL OF MEDICAL GENETICS , vol.46, no.10, pp.663-670, 2009
Otto, E. A. Et Al. 2009. Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11). JOURNAL OF MEDICAL GENETICS , vol.46, no.10 , 663-670.
Otto, E. A., Tory, K., Attanasio, M., Zhou, W., Chaki, M., Paruchuri, Y., ... Wise, E. L.(2009). Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11). JOURNAL OF MEDICAL GENETICS , vol.46, no.10, 663-670.
Otto, E. Et Al. "Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)," JOURNAL OF MEDICAL GENETICS , vol.46, no.10, 663-670, 2009
Otto, E. A. Et Al. "Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)." JOURNAL OF MEDICAL GENETICS , vol.46, no.10, pp.663-670, 2009
Otto, E. A. Et Al. (2009) . "Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)." JOURNAL OF MEDICAL GENETICS , vol.46, no.10, pp.663-670.
@article{article, author={E. A. Otto Et Al. }, title={Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)}, journal={JOURNAL OF MEDICAL GENETICS}, year=2009, pages={663-670} }