by L. S. Bicknell, C. Farrington-Rock, Y. Shafeghati, P. Rump, Y. Alanay, Y. Alembik, N. Al-Madani, H. Firth, M. H. Karimi-Nejad, C. A. Kim, K. Leask, M. Maisenbacher, E. Moran, J. G. Pappas, P. Prontera, T. de Ravel, J. P. Fryns, E. Sweeney, A. Fryer, S. Unger, L. C. Wilson, R. S. Lachman, D. L. Rimoin, D. H. Cohn, D. Krakow, S. P. Robertson
Reference:
L. S. Bicknell, C. Farrington-Rock, Y. Shafeghati, P. Rump, Y. Alanay, Y. Alembik, N. Al-Madani, H. Firth, M. H. Karimi-Nejad, C. A. Kim, K. Leask, M. Maisenbacher, E. Moran, J. G. Pappas, P. Prontera, T. de Ravel, J. P. Fryns, E. Sweeney, A. Fryer, S. Unger, L. C. Wilson, R. S. Lachman, D. L. Rimoin, D. H. Cohn, D. Krakow, S. P. RobertsonA molecular and clinical study of Larsen syndrome caused by mutations in FLNBIn J Med Genet, volume 44, 2007.
Bibtex Entry:
@article{RN2781,
author = {Bicknell, L. S. and Farrington-Rock, C. and Shafeghati, Y. and Rump, P. and Alanay, Y. and Alembik, Y. and Al-Madani, N. and Firth, H. and Karimi-Nejad, M. H. and Kim, C. A. and Leask, K. and Maisenbacher, M. and Moran, E. and Pappas, J. G. and Prontera, P. and de Ravel, T. and Fryns, J. P. and Sweeney, E. and Fryer, A. and Unger, S. and Wilson, L. C. and Lachman, R. S. and Rimoin, D. L. and Cohn, D. H. and Krakow, D. and Robertson, S. P.},
title = {A molecular and clinical study of Larsen syndrome caused by mutations in FLNB},
journal = {J Med Genet},
volume = {44},
number = {2},
pages = {89-98},
url = {Bicknell J Med Genet 2007.pdf},
year = {2007},
type = {Journal Article}
}