Authors: Trummer, T Brenner, R Just, W Vogel, W Kennerknecht, I

Citation: T. Trummer et al., Recurrent mutations in the COL1A2 gene in patients with osteogenesis imperfecta, CLIN GENET, 59(5), 2001, pp. 338-343

Authors: Barbi, G Kennerknecht, I Wohr, G Avramopoulos, D Karadima, G Petersen, MB

Citation: G. Barbi et al., Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype, AM J MED G, 91(2), 2000, pp. 116-122

Authors: Correa-Cerro, LS Kennerknecht, I Just, W Vogel, W Muller, D

Citation: Ls. Correa-cerro et al., The gene for branchio-oculo-facial syndrome does not colocalise to the EYA1-4 genes, J MED GENET, 37(8), 2000, pp. 620-623

Authors: Kennerknecht, I

Citation: I. Kennerknecht, False-negative findings in chorionic villi - Response, PRENAT DIAG, 19(9), 1999, pp. 892-892

Authors: Kennerknecht, I Barbi, G Djalali, M Mehnert, K Schneider, M Terinde, R Vogel, W

Citation: I. Kennerknecht et al., False-negative findings in chorionic villus sampling. An experimental approach and review of the literature, PRENAT DIAG, 18(12), 1998, pp. 1276-1282