Browsing by Author Sarvananthan, N.

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Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmusTarpey, P.; Thomas, S.; Sarvananthan, N.; Mallya, U.; Lisgo, S.; Talbot, C. J.; Roberts, E. O.; Awan, M.; Surendran, M.; McLean, R. J.; Reinecke, R. D.; Langmann, A.; Lindner, S.; Koch, M.; Jain, S.; Woodruff, G.; Gale, R. P.; Bastawrous, A.; Degg, C.; Droutsas, K.; Asproudis, I.; Zubcov, A. A.; Pieh, C.; Veal, C. D.; Machado, R. D.; Backhouse, O. C.; Baumber, L.; Constantinescu, C. S.; Brodsky, M. C.; Hunter, D. G.; Hertle, R. W.; Read, R. J.; Edkins, S.; O'Meara, S.; Parker, A.; Stevens, C.; Teague, J.; Wooster, R.; Futreal, P. A.; Trembath, R. C.; Stratton, M. R.; Raymond, F. L.; Gottlob, I.24-Nov-2015-
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (vol 38, pg 1242, 2006)Tarpey, P.; Thomas, S.; Sarvananthan, N.; Mallya, U.; Lisgo, S.; Talbot, C. J.; Roberts, E. O.; Awan, M.; Surendran, M.; McLean, R. J.; Reinecke, R. D.; Langmann, A.; Lindner, S.; Koch, M.; Jain, S.; Woodruff, G.; Gale, R. P.; Degg, C.; Droutsas, K.; Asproudis, I.; Zubcov, A. A.; Pieh, C.; Veal, C. D.; Machado, R. D.; Backhouse, O. C.; Baumber, L.; Constantinescu, C. S.; Brodsky, M. C.; Hunter, D. G.; Hertle, R. W.; Read, R. J.; Edkins, S.; O'Meara, S.; Parker, A.; Stevens, C.; Teague, J.; Wooster, R.; Futreal, P. A.; Trembath, R. C.; Stratton, M. R.; Raymond, F. L.; Gottlob, I.; Bastawrous, A.24-Nov-2015-