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Results: 4

Authors: Haug, K Kohlschmidt, N Dereser-Dennl, M Zielinski, J Merz, E Schafer, D
Citation: K. Haug et al., Familial fatal fetal cardiomyopathy with isolated myocardial calcifications: A new syndrome?, AM J MED G, 101(3), 2001, pp. 255-258

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: Stegmann, K Ziegler, A Ngo, ETKM Kohlschmidt, N Schroter, B Ermert, A Koch, MC
Citation: K. Stegmann et al., Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the german population and association studies in probands with neural tube defects(NTD), AM J MED G, 87(1), 1999, pp. 23-29
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