Authors: Fritz, B Hallermann, C Olert, J Fuchs, B Bruns, M Aslan, M Schmidt, S Coerdt, W Muntefering, H Rehder, H

Citation: B. Fritz et al., Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH) - Re-evaluation of chromosome aberration rates in early spontaneous abortions, EUR J HUM G, 9(7), 2001, pp. 539-547

Authors: Kriegsmann, J Coerdt, W Kommoss, F Beetz, R Hallermann, C Muntefering, H

Citation: J. Kriegsmann et al., Renal tubular dysgenesis (RTD) - An important cause of the oligohydramnion-sequence - Report of 3 cases and review of the literature, PATH RES PR, 196(12), 2000, pp. 861-865

Authors: Kohlschmidt, N Zielinski, J Brude, E Schafer, D Olert, J Hallermann, C Coerdt, W Arnemann, J

Citation: N. Kohlschmidt et al., Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS), PRENAT DIAG, 20(2), 2000, pp. 152-155

Authors: Hallermann, C Mucher, G Kohlschmidt, N Wellek, B Schumacher, R Bahlmann, F Shahidi-Asl, P Theile, U Rudnik-Schoneborn, SR Munterfering, H Zerres, K

Citation: C. Hallermann et al., Syndrome of autosomal recessive polycystic kidneys with skeletal and facial anomalies is not linked to the ARPKD gene locus on chromosome 6p, AM J MED G, 90(2), 2000, pp. 115-119

Authors: Bahlmann, F Merz, E Hallermann, C Stopfkuchen, H Kramer, W Hofmann, M

Citation: F. Bahlmann et al., Congenital diaphragmatic hernia: ultrasonic measurement of fetal lungs to predict pulmonary hypoplasia, ULTRASOUN O, 14(3), 1999, pp. 162-168

Authors: Merz, E Miric-Tesanic, D Bahlmann, F Weber, G Hallermann, C

Citation: E. Merz et al., Prenatal sonographic chest and lung measurements for predicting severe pulmonary hypoplasia, PRENAT DIAG, 19(7), 1999, pp. 614-619