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