X-autosome and X-Y translocations in female carriers: X-chromosome inactivation easily detectable by 5-ethynyl-2-deoxyuridine (EdU)
Donat, M, Louis, A, Kreskowski, K, Ziegler, M, Weise, A, Schreyer, I, Liehr, T
Characterization of Small Supernumerary Marker Chromosomes By A Simple Molecular and Molecular Cytogenetics Approach
Liehr, T, Trifonov, V, Polityko, A, Brecevic, L, Mrasek, K, Weise, A, Ewers, E, Reich, D, Iourov, I, Mkrtchyan, H, Manvelyan, M, Kosyakova, N
Human Ring Chromosomes – New Insights for their Clinical Significance
Guilherme, R.S., Klein, E, Hamid, A.B., Bhatt, S, Volleth, M, Polityko, A, Kulpanovich, A, Dufke, A, Albrecht, B, Morlot, S, Brecevic, L, Petersen, M.B., Manolakos, E, Kosyakova, N, Liehr, T
Involvement of Chromosomes 7, 18 and X in Mitomycin C-Induced Micronuclei
Hovhannisyan, G, Mkrtchyan, H, Liehr, T, Aroutiounian, R
Evidence for Correlation of Fragile Sites and Chromosomal Breakpoints in Carriers of Constitutional Balanced Chromosomal Rearrangements
Liehr, T, Kosayakova, N, Schröder, J, Ziegler, M, Kreskowski, K, Pohle, B, Bhatt, S, Theuss, L, Wilhelm, K, Weise, A, Mrasek, K
Molecular Analysis of Ring Y Chromosome in a 10-Year-Old Boy with Mixed Gonadal Dysgenesis and Growth Hormone Deficiency
Milenkovic, T, Guc-Scekic, M, Zdravkovic, D, Topic, V, Liehr, T, Joksic, G, Radivojevic, D, Lakic, N
Trisomy 21 with a Small Supernumerary Marker Chromosome Derived from Chromosomes 13/21 and 18
Niksic, S, Deretic, V, Pilic, G, Ewers, E, Merkas, M, Ziegler, M, Liehr, T
Pallister-Killian Syndrome: Rare Phenotypic Features and Variable Karyotypes
Liehr, T, Wegner, R-D, Stumm, M, Joksić, G, Polityko, A, Kosyakova, N, Ewers, E, Reich, D, Wagner, R, Weise, A
The Multicolor Fluorescence in Situ Hybridization (mFISH) Homepage
Liehr, T