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Group by: Item Type | Date
Number of items: 4.

Journal article

Scherag, A.; Kleber, M.; Boes, T.; Kolbe, A. L.; Ruth, A.; Grallert, H.; Illig, T.; Heid, I. M.; Toschke, André Michael; Grau, K.; Sorensen, T. I.; Hebebrand, J.; Hinney, A. and Reinehr, T. (2011): SDCCAG8 Obesity Alleles and Reduced Weight Loss After a Lifestyle Intervention in Overweight Children and Adolescents. In: Obesity (Silver Spring), Vol. 20, No. 2: pp. 466-470

Heid, I. M.; Vollmert, C.; Kronenberg, F.; Huth, C.; Ankerst, Donna Pauler; Luchner, A.; Hinney, A.; Brönner, G.; Wichmann, H. E.; Illig, T.; Döring, A. and Hebebrand, J. (2008): Association of the MC4R V103I polymorphism with the metabolic syndrome: the KORA Study. In: Obesity, Vol. 16, No. 2: pp. 369-376

Vollmert, C.; Windl, O.; Xiang, W.; Rosenberger, A.; Zerr, I.; Wichmann, Heinz-Erich; Bickeböller, H.; Illig, T. and Kretzschmar, Hans A. (2006): Significant association of a M129V independent polymorphism in the 5\prime UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study. In: Journal of Medical Genetics, Vol. 43, No. 10, e53 [PDF, 211kB]

Klopp, N.; Heon, E.; Billingsley, G.; Illig, T.; Wjst, M.; Rudolph, G. and Graw, Jochen (2003): Further genetic heterogeneity for autosomal dominant human sutural cataracts. In: Ophthalmic Research, No. 2: pp. 71-77 [PDF, 246kB]

This list was generated on Sun Feb 18 00:28:23 2024 CET.