Publikationen von Fikret Erdogan

Klopocki, E.; Fiebig, B.; Robinson, P. N.; Tönnies, H.; Erdogan, F.; Ropers, H.-H.; Mundlos, S.; Ullmann, R.: A novel 8 Mb interstitial deletion of chromosome 8p12-p21.2. American Journal of Medical Genetics Part A 140A (8), S. 873 - 877 (2006)

Bækvad-Hansen, M.; Tümer, Z.; Delicado, A.; Erdogan, F.; Tommerup, N.; Larsen, L. A.: Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease. American Journal of Medical Genetics Part A 140 (5), S. 427 - 33 (2006)

Garshasbi, M.; Motazacker, M. M.; Kahrizi, K.; Behjati, F.; Abedini, S. S.; Nieh, S. E.; Firouzabadi, S. G.; Becker, C.; Rüschendorf, F.; Nürnberg, P. et al.; Tzschach, A.; Vazifehmand, R.; Erdogan, F.; Ullmann, R.; Lenzner, S.; Kuss, A. W.; Ropers, H.-H.; Najmabadi, H.: SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly. Human Genetics 118 (6), S. 708 - 715 (2006)

Chen, W.; Erdogan, F.; Ropers, H.-H.; Lenzner, S.; Ullmann, R.: : CGHPRO – a comprehensive data analysis tool for array CGH. BMC Bioinformatics 6 (1), S. 1471 - 2105 (2005)

Erdogan, F.: Typisierung biallelischer Marker (SNPs) mit DNS-Mikrorastern. Dissertation, Freie Universtität Berlin, Berlin (2003)