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pro vyhledávání: '"Luijten, M. N. H."'
Autor:
Luijten, M. N. H., Basten, S. G., Claessens, T., Vernooij, M., Scott, C. L., Janssen, R., Easton, J. A., Kamps, M. A. F., Vreeburg, M., Broers, J. L. V., van Geel, M., Menko, F. H., Harbottle, R. P., Nookala, R. K., Tee, A. R., Land, S. C., Giles, R. H., Coull, B. J., van Steensel, M. A. M.
Publikováno v:
Human Molecular Genetics, 22(21), 4383-4397. Oxford University Press
Luijten, M N H, Basten, S G, Claessens, T, Vernooij, M, Scott, C L, Janssen, R, Easton, J A, Kamps, M A F, Vreeburg, M, Broers, J L V, Van Geel, M, Menko, F H, Harbottle, R P, Nookala, R K, Tee, A R, Land, S C, Giles, R H, Coull, B J & van Steensel, M A M 2013, ' Birt-Hogg-Dube syndrome is a novel ciliopathy ', Human Molecular Genetics, vol. 22, no. 21, pp. 4383-4397 . https://doi.org/10.1093/hmg/ddt288
Human Molecular Genetics; Vol 22
Luijten, M N H, Basten, S G, Claessens, T, Vernooij, M, Scott, C L, Janssen, R, Easton, J A, Kamps, M A F, Vreeburg, M, Broers, J L V, Van Geel, M, Menko, F H, Harbottle, R P, Nookala, R K, Tee, A R, Land, S C, Giles, R H, Coull, B J & van Steensel, M A M 2013, ' Birt-Hogg-Dube syndrome is a novel ciliopathy ', Human Molecular Genetics, vol. 22, no. 21, pp. 4383-4397 . https://doi.org/10.1093/hmg/ddt288
Human Molecular Genetics; Vol 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4cab7ab7a3e19ff3170ef50fe45f1102
https://research.vumc.nl/en/publications/b03b0237-a0e9-4ce7-9bd9-be661f75621f
https://research.vumc.nl/en/publications/b03b0237-a0e9-4ce7-9bd9-be661f75621f