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Bens, Susanne; Haake, Andrea; Richter, Julia et al.

Frequency and characterization of DNA methylation defects in children born SGA

EUROPEAN JOURNAL OF HUMAN GENETICS. Bd. 21. H. 8. 2013 S. 838-843


Burgdörfer, E; Korenkov, M; Jonas, D et al.

FTO and INSIG2 genotyping combined with metabolic and anthropometric phenotyping of morbidly obese patients

Mol Syndromol. Bd. 4. H. 6. 2013 S. 273-279


Yildiz, Yildiz; Hoffmann, Per; vom Dahl, Stefan et al.

Functional and genetic characterization of the non-lysosomal glucosylceramidase 2 as a modifier for Gaucher disease

ORPHANET JOURNAL OF RARE DISEASES. Bd. 8. 2013


Lukas, Jan; Giese, Anne-Katrin; Markoff, Arseni et al.

Functional Characterisation of Alpha-Galactosidase A Mutations as a Basis for a New Classification System in Fabry Disease

PLOS GENETICS. Bd. 9. H. 8. 2013


Knauer, Shirley K.; Unruhe, Britta; Karczewski, Sarah et al.

Functional Characterization of Novel Mutations Affecting Survivin (BIRC5)-Mediated Therapy Resistance in Head and Neck Cancer Patients

HUMAN MUTATION. Bd. 34. H. 2. 2013 S. 395-404


Mutschler, Jochen; Abbruzzese, Elvira; Wiedemann, Klaus et al.

Functional Polymorphism in the Neuropeptide Y Gene Promoter (rs16147) Is Associated with Serum Leptin Levels and Waist-Hip Ratio in Women

ANNALS OF NUTRITION AND METABOLISM. Bd. 62. H. 4. 2013 S. 271-276


Wagner, E. M.; Schaefer, L.; Bopp, T. et al.

Functionally-altered GPI-anchor-negative Treg following alemtuzumab-based T-cell depletion are associated with acute GVHD

BONE MARROW TRANSPLANTATION. Bd. 48. 2013 S. S172-S172


Burgmaier, Mathias; Barroso, Michael T. Coll; Custodis, Florian et al.

Funding: German Cardiac Research Foundation

CIRCULATION. Bd. 127. H. 16. 2013 S. F91-F96