Zobrazeno 1 - 10
of 608
pro vyhledávání: '"Frants, R.R"'
Autor:
Kaja, S., van de Ven, R.C.G., Broos, L.A.M., Frants, R.R., Ferrari, M.D., van den Maagdenberg, A.M.J.M., Plomp, J.J.
Publikováno v:
In Neuroscience 2007 144(4):1278-1287
Autor:
van der Kooi, E.L., de Greef, J.C., Wohlgemuth, M., Frants, R.R., van Asseldonk, R.J.G.P., Blom, H.J., van Engelen, B.G.M., van der Maarel, S.M., Padberg, G.W.
Publikováno v:
In Neuromuscular Disorders 2006 16(11):766-769
Autor:
Kaja, S., van de Ven, R.C.G., Broos, L.A.M., Veldman, H., van Dijk, J.G., Verschuuren, J.J.G.M., Frants, R.R., Ferrari, M.D., van den Maagdenberg, A.M.J.M., Plomp, J.J.
Publikováno v:
In Neuroscience 2005 135(1):81-95
Autor:
Krom, Y.D., Gras, J.C.E., Frants, R.R., Havekes, L.M., van Berkel, T.J., Biessen, E.A.L., van Dijk, K. Willems
Publikováno v:
In Biochemical and Biophysical Research Communications 2005 338(2):847-854
Genome-wide association studies have discovered hundreds of loci associated with complex brain disorders, but it remains unclear in which cell types these loci are active. Here we integrate genome-wide association study results with single-cell trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::8da5727df8072905eec14c2619c9f167
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3077430
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3077430
Autor:
van Koningsbruggen, S., de Haard, H., de Kievit, P., Dirks, R.W., van Remoortere, A., Groot, A.J., van Engelen, B.G.M., den Dunnen, J.T., Verrips, C.T., Frants, R.R., van der Maarel, S.M. *
Publikováno v:
In Journal of Immunological Methods 2003 279(1):149-161
Publikováno v:
In Biochemical and Biophysical Research Communications 14 July 2000 273(3):1084-1087
Publikováno v:
In Genomics 1 October 1999 61(1):55-65
Publikováno v:
Human Heredity, 1988 Jan 01. 38(5), 277-282.
Externí odkaz:
https://www.jstor.org/stable/45102216
Autor:
Kievit, P. de, Geel, M. van, Wielen, M.J.R. van der, Bakker, E., Padberg, G.W.A.M., Frants, R.R., Maarel, S.M. van der
Publikováno v:
Annals of Neurology, 50, 6, pp. 816--9
Annals of Neurology, 50, 816--9
Annals of Neurology, 50, 816--9
Item does not contain fulltext Facioscapulohumeral muscular dystrophy is caused by partial deletion of the D4Z4 repeat array on chromosome 4q35. Genetic diagnosis is based on sizing of this repeat array, which is complicated by cross-hybridization of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::37d21268777dc5a0c0c63c8228f472d7
https://hdl.handle.net/2066/185593
https://hdl.handle.net/2066/185593