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Metabolic Programming of MEST DNA Methylation by Intrauterine Exposure to Gestational Diabetes MellitusDIABETES. Bd. 62. H. 4. 2013 S. 1320-1328
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Novel VANGL 1 Gene Mutations in 144 Slovakian , Romanian and German Patients with Neural Tube DefectsMolecular syndromology. Bd. 3. H. 2. 2013 S. 76-81
Lehnen, H.; Mosblech, N.; Reineke, T. et al.
Prenatal Clinical Assessment of sFlt-1 (Soluble fms-like Tyrosine Kinase-1)/PlGF (Placental Growth Factor) Ratio as a Diagnostic Tool for Preeclampsia, Pregnancy-induced Hypertension, and ProteinuriaGEBURTSHILFE UND FRAUENHEILKUNDE. Bd. 73. H. 5. 2013 S. 440-445
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Searching for Gene Expression Differences in Primary Fibroblasts Between Patients with One and Two Neoplasms in ChildhoodPEDIATRIC HEMATOLOGY AND ONCOLOGY. Bd. 30. H. 1. 2013 S. 33-45
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Sirtuin-6-Dependent Genetic and Epigenetic Alterations Are Associated With Poor Clinical Outcome in Hepatocellular Carcinoma PatientsHEPATOLOGY. Bd. 58. H. 3. 2013 S. 1054-1064
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Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnosticsBMJ OPEN. Bd. 3. H. 3. 2013
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Stochastic Loss of Silencing of the Imprinted Ndn/NDN Allele, in a Mouse Model and Humans with Prader-Willi Syndrome, Has Functional ConsequencesPLOS GENETICS. Bd. 9. H. 9. 2013
Fatima, Azra; Shao Kaifeng, ?; Dittmann, Sven et al.
The Disease-Specific Phenotype in Cardiomyocytes Derived from Induced Pluripotent Stem Cells of Two Long QT Syndrome Type 3 PatientsPLOS ONE. Bd. 8. H. 12. 2013
Linke, M.; May, A.; Reifenberg, K. et al.
The Impact of Ovarian Stimulation on the Expression of Candidate Reprogramming Genes in Mouse Preimplantation EmbryosCYTOGENETIC AND GENOME RESEARCH. Bd. 139. H. 2. 2013 S. 71-79
Ziebart, Thomas; Draenert, Florian G.; Galetzka, Danuta et al.
The original family revisited after 37 years: odontoma-dysphagia syndrome is most likely caused by a microduplication of chromosome 11q13.3, including the FGF3 and FGF4 genesCLINICAL ORAL INVESTIGATIONS. Bd. 17. H. 1. 2013 S. 123-130