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1. Vergleichende molekularbiologische Untersuchung des IGHMBP2-Gens bei Patienten mit plötzlichem Säuglingstod (SIDS) und Säuglingen mit erklärter Todesursache (non-SIDS) ;...


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2. Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability ; the WASH complex member SWIP ; Identifikation eines neuen Krankheitgens...


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3. Untersuchungen der tri-/quatroallelen Serotonintransporter-Promoter-Region (5-HTTLPR) auf Assoziation mit depressions-relevanten Phänotypen ; Analysis of the tri-/quatroallelic...


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4. Nijmegen Breakage Syndrom (NBS) ; Krebsrisiko bei Heterozygotie für die Mutationen 657del5 und R215W ; Nijmegen Breakage Syndrome (NBS) ; cancer risk and heterozygosity for the...


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5. Molecular genetic and cytogenetic analyses of autosomal recessive primary microcephaly (MCPH) ; mouse model, new locus and novel mutations ; Molekular- und zytogenetische...


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6. Assoziationsstudie zur klinischen Variabilität bei Patienten mit dem Nijmegen Breakage Syndrom ; Association study to the clinical variability in the patients with Nijmegen...


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7. INFORMATION DISTRIBUTION IN COMPLEX SYSTEMS TO IMPROVE TEAM PERFORMANCE

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8. Mutationsanalyse im NBS1-Gen bei Patientinnen mit BRCA1/2 negativem familiären und BRCA1/2 negativem sporadischen Mammakarzinom ; Mutation analysis in the NBS1 gene in patients...


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9. 129Xe-NMR of carbon black filled elastomers


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10. REGULATION OF THE 5-LIPOXYGENASE PATHWAY IN HUMAN LEUCOCYTES


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