Zobrazeno 1 - 4
of 4
pro vyhledávání: '"E J, Meershoek"'
Autor:
G.J.B. van Ommen, A C Chinault, S. Wang, Bart W. Nieuwenhuijsen, E. J. Meershoek, V.H. Fischbeck, K.L. Chen, V.H. Valmiki
Publikováno v:
Human Molecular Genetics. 1:605-612
A contiguous set of 43 overlapping yeast artificial chromosome (YAC) clones has been developed for the Charcot-Marie-Tooth disease type 1A (CMT1A) duplication region of chromosome 17p11.2. The contig spans approximately 2.0 Mb and can be represented
Autor:
N A, Datson, E, Semina, A A, van Staalduinen, H G, Dauwerse, E J, Meershoek, J J, Heus, R R, Frants, J T, den Dunnen, J C, Murray, G J, van Ommen
Publikováno v:
American journal of human genetics. 59(6)
Rieger syndrome (RGS) is an autosomal dominant disorder of morphogenesis affecting mainly the formation of the anterior eye chamber and of the teeth. RGS has been localized to human chromosome 4q25 by linkage to epidermal growth factor (EGF). We have
Autor:
David E. Housman, Frank Baas, Vincent P. Stanton, Linda J. Valentijn, N H van den Bosch, G. W. Hensels, Garth A. Nicholson, E. J. Meershoek, I. Zorn, G.J.B. van Ommen, Kenneth H. Fischbeck, Hans G. Dauwerse, D. A. Ross, Pieter A. Bolhuis, Jessica E. Hoogendijk
Publikováno v:
Nature genetics, 1(3), 166-170. Nature Publishing Group
Charcot-Marie-Tooth disease type 1A (CMT1A) is associated with a DNA duplication at chromosome 17p11.2. In view of the point mutation in the gene for peripheral myelin protein pmp-22/gas-3 in Trembler mice, a murine model for CMT1A, we have analysed
Autor:
G.J.B. van Ommen, Kenneth H. Fischbeck, E. J. Meershoek, K.L. Chen, M.S. Driesen, P. Mollevanger, Martin C. Wapenaar, J. G. Dauwerse
Publikováno v:
Genomics. 11(4)
A yeast artificial chromosome (YAC) library has been constructed from a somatic cell hybrid containing a t(1p;19q) chromosome and chromosome 17. After amplification, part of this library was analyzed by high-density colony filter screening with a rep