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Citation: W. Scheurlen et al., Chronic autoimmune thrombopenia/neutropenia in a boy with persistent parvovirus B19 infection, J CLIN VIRO, 20(3), 2001, pp. 173-178

Authors: Hoglund, P Sormaala, M Haila, S Socha, J Rajaram, U Scheurlen, W Sinaasappel, M de Jonge, H Holmberg, C Yoshikawa, H Kere, J

Citation: P. Hoglund et al., Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea, HUM MUTAT, 18(3), 2001, pp. 233-242

Authors: Granzow, M Popp, S Weber, S Schoell, B Holtgreve-Grez, H Senf, L Hager, D Boschert, J Scheurlen, W Jauch, A

Citation: M. Granzow et al., Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics, CANC GENET, 130(1), 2001, pp. 79-83

Authors: Otano-Joos, M Mechtersheimer, G Ohl, S Wilgenbus, KK Scheurlen, W Lehnert, T Willeke, F Otto, HF Lichter, P Joos, S

Citation: M. Otano-joos et al., Detection of chromosomal imbalances in leiomyosarcoma by comparative genomic hybridization and interphase cytogenetics, CYTOG C GEN, 90(1-2), 2000, pp. 86-92

Authors: Rutkowski, S Scheurlen, W Girschick, H Schuster, V

Citation: S. Rutkowski et al., Agranulocytosis in a 15-months old girl: congenital neutropenia or cyclic neutropenia, MONATS KIND, 147(11), 1999, pp. 1018-1022