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Zeitschriftenartikel (4)

Meierhofer, D.; Mayr, J. A.; Ebner, S.; Sperl, W.; Kofler, B.: Rapid screening of the entire mitochondrial DNA for low-level heteroplasmic mutations. Mitochondrion 5 (4), S. 282 - 296 (2005)
Zi, Z.; Cho, K.-H.; Sung, M.-H.; Xia, X.; Zheng, J.; Sun, Z.: In silico identification of the key components and steps in IFN-γ induced JAK-STAT signaling pathway. FEBS Letters 579 (5), S. 1101 - 1108 (2005)
Boonen, S. E.; Stahl, D.; Kreiborg, S.; Rosenberg, T.; Kalscheuer, V.; Larsen, L. A.; Tommerup, N.; Brondum-Nielsen, K.; Tumer, Z.: Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome. Am J Med Genet A 132A (3), S. 324 - 8 (2005)
Tumer, Z.; Henriksen, A. M.; Bache, I.; Brixen, K.; Kalscheuer, V.; Illum, N.; Rasmussen, K.; Larsen, L. A.; Tommerup, N.: Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome. Am J Med Genet A 135 (3), S. 339 - 41 (2005)
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