Institute of Medical Genetics CVK

Projects

• Analysis of phenotypic and functional variances of lamin B receptor mutations
• Analysis of the Growth and Differentiation Factor 5 and its site-directed modification for therapeutic applications
• Analysis of the Receptor Tyrosine Kinase Ror2: A Paradigm for Phenotypic Variation in Allelic Genetic Disorders.
• Charakterisierung d. Cohen-Syndroms
• Clinical and functional characterization of mutation in the GDF5/BMPR1B-pathway
• Cohen - Syndrome
• Craniometaphyseal Dysplasia - Clinical Variability and Pathogenic Pathways
• Die Molekularbiologie der Frakturheilung
• Klin. Forschergruppe TP 9 - 4
• Microarray-based comparative Genomic Hybridization
• Molecular Pathology and Embryology of HOXD-related Limb Malformations
• NF1-flanking Genes

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