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Klinische Monatsblatter Fur Augenheilkunde|May 21, 1998
[Type I lattice corneal dystrophy. Clinical and molecular genetic study of a large family]M Meins, M Kohlhaas, G Richard, et al.Human Mutation|March 10, 2001
Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regionsF Laccone, P Huppke, F Hanefeld, et al.The Journal of Biological Chemistry|September 15, 1988
Glucose permease of Escherichia coli. Purification of the IIGlc subunit and functional characterization of its oligomeric formsM Meins, B Zanolari, J P Rosenbusch, et al.Genomics|August 11, 2000
Characterization of the human TBX20 gene, a new member of the T-Box gene family closely related to the Drosophila H15 geneM Meins, D J Henderson, S S Bhattacharya, et al.Neuropediatrics|October 9, 2002
Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patientsM Meins, K Brockmann, S Yadav, et al.American Journal of Human Genetics|April 20, 2001
MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal originR Trappe, F Laccone, J Cobilanschi, et al.The Journal of Biological Chemistry|June 5, 1993
Cysteine phosphorylation of the glucose transporter of Escherichia coliM Meins, P Jenö, D Müller, et al.Investigative Ophthalmology & Visual Science|December 1, 2001
Expression of Drosophila omb-related T-box genes in the developing human and mouse neural retinaJ C Sowden, J K Holt, M Meins, et al.Human Mutation|January 4, 2001
Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysisI Zwaenepoel, E Verpy, S Blanchard, et al.Development (Cambridge, England)|December 1, 1993
Variable and multiple expression of Protease Nexin-1 during mouse organogenesis and nervous system developmentI M Mansuy, H van der Putten, P Schmid, et al.Pageof 3