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