2. Material und Methoden - ArchiMeD

LITERATURVERZEICHNIS
WILCOX, A. S.; KHAN, A. S.; HOPKINS, J. A.; SIKELA, J. M. (1991). Use of 3´ untranslated
sequences of human cDNAs for rapid chromosome assignment and conversion to STSs:
impliction for an expression map of the genome. Nucl. Acids Res. 19: 1837-1842.
WILKIE, A. O. M.; SLANEY, S. F.; OLDRIDGE, M.; POOLE, M. D.; ASHWORTH, G. J.;
HOCKLEY, A. D.; HAYWARD, R. D.; DAVID, D. J.; PULLEYN, L. J.; RUTLAND, P.;
MALCOLM, S.; WINTER, R. M.; REARDON, W. (1995). Apert Syndrome results from
localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nat. Genet. 9: 165-168.
WILKIE, A. O. M.; MORRISS-KAY, G. M.; JONES, E. Y.; HEATH, J.K. (1995). Functions of
fibroblast growth factors and their receptors. Curr. Biol. 5: 500-507.
WINTERPACHT, A.; HILBERT, K.; STELZER, C.; SCHWEIKARDT, T.; DECKER, H.;
SEGERER, H.; SPRANGER, J.; ZABEL, B. (2000). A novel mutation in FGFR-3 disrupts a
putative N-glycosylation site and results in hypochondroplasia. Physiol. Genomics 2: 9-12.
WUECHNER, C.; HILBERT, K.; ZABEL, B.; WINTERPACHT, A (1997): Human fibroblast growth
factor receptor 3 gene (FGFR3): genomic sequence and primer set information for gene
analysis. Hum. Genet. 100: 215-219.
ZABEL, B. U. UND WINTERPACHT, A. (2000), Osteochondrodysplasien - genetisch bedingte
Störungen der Skelettentwicklung. In: Ganten, D. und Ruckpaul, K. (Hrsg.) Handbuch der
molekularen Medizin, Band 7: Monogen bedingte Erbkrankheiten, Teil 2. Springer Verlag
Berlin, Heidelberg, New York (im Druck).
ZGURICASA, J.; HEUSB, H.; MORALES-PERALTAC, E.; BREEDVELDB, G.; KUYTD, B.;
MUMCUE, E. F.; BAKKERA, W.; AKARSUF, N.; KAYG, S. P. J.; HOVIUSA,S. E. R.;
HEREDERO-BAUTEC, L.; OOSTRAB, B. A.; HEUTINK, P (1999). Clinical and genetic
studies on 12 preaxial polydactyly families and refinement of the localisation of the gene
responsible to a 1.9 cM region on chromosome 7q36. J. Med. Genet 36, 33-40.
ZHANG, H. CATRON, K. M.; ABATE-SHEN, C. (1996). A role for the Msx-1 homeodomain in
transcriptional regulation: Residues in the N-terminal arm mediate TATA binding protein
interaction and transcriptional repression. Proc. Natl. Acad. Sci. U.S.A. 93: 1764-1769.
ZHANG, L.; ZHOU, W.; VELCULESCU, V. E.; KERN, S. E.; HRUBAN, R. H.; HAMILTON, S. R.;
VOGELSTEIN, B.; KINZLER, K. W. (1997). Gene expression profiles in normal and cancer
cells. Science 276: 1268-1272.
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