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Citation: H. Bolz et al., Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D, NAT GENET, 27(1), 2001, pp. 108-112

Authors: Kutsche, K Yntema, H Brandt, A Jantke, I Nothwang, HG Orth, U Boavida, MG David, D Chelly, J Fryns, JP Moraine, C Ropers, HH Hamel, BCJ van Bokhoven, H Gal, A

Citation: K. Kutsche et al., Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation, NAT GENET, 26(2), 2000, pp. 247-250

Authors: Kutsche, K Glauner, E Knauf, S Pomarino, A Schmidt, M Schroder, B Nothwang, HG Schuler, HM Goecke, TO Kersten, AJ Althaus, C Gal, A

Citation: K. Kutsche et al., Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium, CYTOG C GEN, 91(1-4), 2000, pp. 141-147

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Citation: T. Schlake et al., Predetermined chromosomal deletion encompassing the Nf-1 gene, ONCOGENE, 18(44), 1999, pp. 6078-6082