Institute of Human Genetics CVK

Projects

• Analysis of the pathogenesis of a new autosomal recessive disease with premature chromosome condensation
• AnEUploidy
• AnEUploidy
• chrom. Instabilität bei Tumorentstehung
• Chromosome condensation
• Clonal aberrations Fanconi anemia
• Clonal chromosome aberrations
• Congenital Eye Diseases
• Decision of induced abortion after PND
• DNA Reparaturproteine Nibrin und FANCA
• DNA-Methylation profiling in healthy children conceived by assisted reproduction (ART)
• Ermittlung prognostischer Fak
• Fanconi anemia: clonal chromosome aberrations in bone marrow cells with respect to prognosis
• Funktionsanalyse des menschlichen hSNM1B-Gens
• GRK 754/3 TP 10
• hSNM1B-Gens
• Molecular Basis of Clinical Variability in Mendelian Disorders
• Proteome Networking
• Stipendienprogramm der Gottlieb Daimler Stiftung
• The Nijemgen Breakage Syndrom (NBS) belongs to a group of disorders the genes of which function in a protein comple
• Understanding the chronic neurological alterations of down syndrome
• Untersuchung Mäusestämme
• Vorsorgungsoptimierung für Frauen mit erblicher Belastung für Brustkrebs

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