Authors: Richter, B Stegmann, K Roper, B Boddeker, I Ngo, ETKM Koch, MC

Citation: B. Richter et al., Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population, J HUM GENET, 46(3), 2001, pp. 105-109

Authors: Stegmann, K Boecker, J Richter, B Capra, V Finnell, RH Ngo, ETKN Strehl, E Ermert, A Koch, MC

Citation: K. Stegmann et al., A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects, TERATOLOGY, 63(5), 2001, pp. 167-175

Authors: Busse, K Kohler, J Stegmann, K Pongratz, D Koch, MC Schreiber, H

Citation: K. Busse et al., An inherited 4q35-EcoRI-DNA-fragment of 35 kb in a family with a sporadic case of facioscapulohumeral muscular dystrophy (FSHD), NEUROMUSC D, 10(3), 2000, pp. 178-181

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