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Gao, B.; Hu, J.; Stricker, S.; Cheung, M.; Ma, G.; Law, K. F.; Witte, F.; Briscoe, J.; Mundlos, S.; He, L. et al.; Cheah, K. S. E.; Chan, D.: A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range. Nature 458 (7242), pp. 1196 - 1200 (2009)

Zerck, A.; Nordhoff, E.; Resemann, A.; Mirgorodskaya, E.; Suckau, D.; Reinert, K.; Lehrach, H.; Gobom, J.: An Iterative Strategy for Precursor Ion Selection for LC-MS/MS Based Shotgun Proteomics. Journal of Proteome Research 8 (7), pp. 3239 - 3251 (2009)

Jogler, C.; Lin, W.; Meyerdierks, A.; Kube, M.; Katzmann, E.; Flies, C.; Pan, Y.; Amann, R.; Reinhard, R.; Schüler, D.: Toward Cloning of the Magnetotactic Metagenome: Identification of Magnetosome Island Gene Clusters in Uncultivated Magnetotactic Bacteria from Different Aquatic Sediments. Applied and Environmental Microbiology 75 (12), pp. 3972 - 3979 (2009)

Ralser, M.; Zeidler, U.; Lehrach, H.: Interfering with Glycolysis Causes Sir2-Dependent Hyper-Recombination of Saccharomyces cerevisiae Plasmids. PLoS ONE 4 (4), p. e5376 - e5376 (2009)

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Fu, X.; Fu, N.; Guo, S.; Yan, Z.; Xu, Y.; Hu, H.; Menzel, C.; Chen, W.; Li, Y.; Zeng, R. et al.; Khaitovich, P.: Estimating accuracy of RNA-Seq and microarrays with proteomics. BMC Genomics 10, p. 161 - 161 (2009)

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Baek, Y.-S.; Haas, S.; Hackstein, H.; Bein, G.; Hernandez-Santana, M.; Lehrach, H.; Sauer, S.; Seitz, H.: Identification of novel transcriptional regulators involved in macrophage differentiation and activation in U937 cells. BMC Immunology 10, p. 18 - 18 (2009)

Graul-Neumann, L. M.; Stieler, K. M.; Blume-Peytavi, U.; Tzschach, A.: Autosomal dominant inheritance in a large family with focal facial dermal dysplasia (Brauer-Setleis syndrome). American Journal of Medical Genetics Part A 149 (4), pp. 746 - 750 (2009)

Lugtenberg, D.; Kleefstra, T.; Oudakker, A. R.; Nillesen, W. M.; Yntema, H. G.; Tzschach, A.; Raynaud, M.; Rating, D.; Journel, H.; Chelly, J. et al.; Goizet, C.; Lacombe, D.; Pedespan, J.-M.; Echenne, B.; Tariverdian, G.; O'Rourke, D.; King, M. D.; Green, A.; van Kogelenberg, M.; Van Esch, H.; Gecz, J.; Hamel, B. C. J.; van Bokhoven, H.; de Brouwer, A. P. M.: Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy. European Journal of Human Genetics 17 (4), pp. 444 - 453 (2009)

Mangerich, A.; Scherthan, H.; Diefenbach, J.; Kloz, U.; van der Hoeven, F.; Beneke, S.; Bürkle, A.: A caveat in mouse genetic engineering: ectopic gene targeting in ES cells by bidirectional extension of the homology arms of a gene replacement vector carrying human PARP-1. Transgenic Research 18 (2), pp. 261 - 279 (2009)

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Pouya, A. R.; Abedini, S. S.; Mansoorian, N.; Behjati, F.; Nikzat, N.; Mohseni, M.; Nieh, S. E.; Moheb, L. A.; Darvish, H.; Monajemi, G. B. et al.; Banihashemi, S.; Kahrizi, K.; Ropers, H.-H.; Najmabadi, H.: Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population. European Journal of Medical Genetics 52 (4), pp. 170 - 173 (2009)

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Witte, F.; Dokas, J.; Neuendorf, F.; Mundlos, S.; Stricker, S.: Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation. Gene Expression Patterns 9 (4), pp. 215 - 223 (2009)

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