Zobrazeno 1 - 3
of 3
pro vyhledávání: '"H. T. F. M. Verzijl"'
Autor:
Christine Oley, Jennifer M. Kwon, Murray Hargrave, Toshiya Yamada, Vincent Timmerman, Peter Koopman, Carmel Toomes, P. De Jonghe, K.M Nield, Melissa H. Little, Hannie Kremer, Michael J. Dixon, H. T. F. M. Verzijl, Kristy M. James, Kylie Georgas, Timothy J. Sullivan
Publikováno v:
Human genetics
Human Genetics, 106, pp. 432-439
Human Genetics, 106, 432-439
Human Genetics, 106, pp. 432-439
Human Genetics, 106, 432-439
Members of the Sox gene family encode transcription factors that have diverse and important functions during development. We have recently described the cloning of chick and mouse Sox14 and the expression of these genes in a population of ventral int
Autor:
Jeroen Luyten, Gerry Steenbergen, H. T. F. M. Verzijl, George W. Padberg, Ron A. Wevers, L.P.W.J. van den Heuvel, H.J. ter Laak, B.G.M. van Engelen
Publikováno v:
Annals of Neurology, 44, 140-143
Annals of Neurology, 44, 1, pp. 140-143
Annals of Neurology, 44, 1, pp. 140-143
Two types of myoadenylate deaminase (MAD) deficiency have been described, primary or inherited, and secondary or acquired MAD deficiency. In this study, we investigated whether secondary MAD deficiency is indeed acquired or merely coincidental. We de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::678899daa2eea2f1a301bb93b801dbb6
http://hdl.handle.net/2066/257825
http://hdl.handle.net/2066/257825
Autor:
H. T. F. M. Verzijl, B. G. M. Van Engelen, J. A. F. M. Luyten, G. C. H. Steenbergen, L. P. W. J. Van Den Heuvel, H. J. Ter Laak, G. W. Padberg, R. A. Wevers
Publikováno v:
Annals of Neurology. 45:548-548