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Results: 1-10 |
Results: 10
Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population
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
Myotonic dystrophy associated with VACTERL? A case report
Authors: Kolker, S Degen, I Koch, MC Lindner, M Haas, D Hoffmann, GF
Citation: S. Kolker et al., Myotonic dystrophy associated with VACTERL? A case report, NEUROPEDIAT, 32(1), 2001, pp. 53-54
The first case of HCV seroconversion in Portugal after the introduction ofHCVNAT screening
Authors: Araujo, FM Henriques, I Monteiro, F Meireles, E Koch, MC Celeste, R Cunha-Ribeiro, LM
Citation: Fm. Araujo et al., The first case of HCV seroconversion in Portugal after the introduction ofHCVNAT screening, TRANSFUSION, 41(6), 2001, pp. 848-849
A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects
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
Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2)
Authors: Kress, W Mueller-Myhsok, B Ricker, K Schneider, C Koch, MC Toyka, KV Mueller, CR Grimm, T
Citation: W. Kress et al., Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2), NEUROMUSC D, 10(7), 2000, pp. 478-480
An inherited 4q35-EcoRI-DNA-fragment of 35 kb in a family with a sporadic case of facioscapulohumeral muscular dystrophy (FSHD)
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
Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the german population and association studies in probands with neural tube defects(NTD)
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
Linkage of proximal myotonic myopathy to chromosome 3q
Authors: Ricker, K Grimm, T Koch, MC Schneider, C Kress, W Reimers, CD Schulte-Mattler, W Mueller-Myhsok, B Toyka, KV Mueller, CR
Citation: K. Ricker et al., Linkage of proximal myotonic myopathy to chromosome 3q, NEUROLOGY, 52(1), 1999, pp. 170-171
Evaluation of the facioscapulohumeral muscular dystrophy (FSHD1) phenotypein correlation to the concurrence of 4q35 and 10q26 fragments
Authors: Kohler, J Rohrig, D Bathke, KD Koch, MC
Citation: J. Kohler et al., Evaluation of the facioscapulohumeral muscular dystrophy (FSHD1) phenotypein correlation to the concurrence of 4q35 and 10q26 fragments, CLIN GENET, 55(2), 1999, pp. 88-94
Haemophilia and HIV-1 and/or HIV-2 infection. The role of polymorphisms inchemokines and chemokines receptors genes
Authors: Araujo, F Miranda, M Koch, MC Henriques, I Lacerda, P Meireles, E Monteiro, E Cunha-Ribeiro, LM
Citation: F. Araujo et al., Haemophilia and HIV-1 and/or HIV-2 infection. The role of polymorphisms inchemokines and chemokines receptors genes, SEVENTH EUROPEAN CONFERENCE ON CLINICAL ASPECTS AND TREATMENT OF HIV-INFECTION, 1999, pp. 25-28
Risultati: 1-10 |