Alma Küchler

New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome

D. Wieczorek, T. Eggermann, B. Horsthemke, 2017, European Journal of Human Genetics.

Giant congenital melanocytic naevus caused by NRAS Q61K mosaicism

M. Zenker, I. Wieland, K. Griewank, 2022, JEADV Clinical Practice.

Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID

T. Wieland, T. Strom, D. Wieczorek, 2017, European Journal of Human Genetics.

Clinical and molecular characterization of two patients with overlapping de novo microdeletions in 2p14-p15 and mild mental retardation.

S. Kjaergaard, M. Kirchhoff, E. Wohlleber, 2011, European journal of medical genetics.

The gut fermentation product butyrate, a chemopreventive agent, suppresses glutathione S-transferase theta (hGSTT1) and cell growth more in human colon adenoma (LT97) than tumor (HT29) cells

T. Liehr, B. Marian, W. Peters, 2005, Journal of Cancer Research and Clinical Oncology.

Presence of harmless small supernumerary marker chromosomes hampers molecular genetic diagnosis: a case report.

J. Hentschel, K. Mrasek, T. Liehr, 2010, Molecular Medicine Reports.