1. Crolla JA. FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature. Am J Med Genet 1998; 75(4): 367-381.
2. Crolla JA, Long F, Rivera H, Dennis NR. FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases. Am J Med Genet 1998; 75(4): 355-366.
3. Chudoba I, Franke Y, Senger G, Sauerbrei G, Demuth S, Beensen V, Neumann A, Hansmann I, Claussen U. Maternal UPD 20 in a hyperactive child with severe growth retardation. Eur J Hum Genet 1999; 7(5): 33-40.
4. Kotzot D. Abnormal phenotypes in uniparental disomy (UPD): fundamental aspects and a critical review with bibliography of UPD other than 15. Am J Med Genet 1999; 82(3): 265-274.
5. Kotzot D. Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements. J Med Genet 2001; 38(8): 497-507.
6. Verma RS, Babu A. Human Chromosomes – Manual of Basic Techniques. New York: Pergamon Press, 1989.
7. Liehr T, Thoma K, Kammler K, Gehring C, Ekici A, Bathke KD, Grehl H, Rautenstrauss B. Direct preparation of uncultured EDTA-treated or heparinized blood for interphase FISH analysis. Appl Cytogenet 1995; 21(6): 185-188.
8. Nietzel A, Rocchi M, Starke H, Heller A, Fiedler W, Wlodarska I, Loncarevic I, Beensen V, Claussen U, Liehr T. A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH). Hum Genet 2001; 108(3): 199-204.
9. Trifonov V, Seidel J, Starke H, Prechtel M, Beensen V, Ziegler M, Hartmann I, Heller A, Nietzel A, Claussen U, Liehr U. Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter. Prenat Diagn 2003; in press.
10. Starke H, Nietzel A, Weise A, Heller A, Mrasek K, Belitz B, Kelbova C, Volleth M, Albrecht B, Mitulla B, Trappe R, Bartels I, Adolph S, Dufke A, Singer S, Stumm M, Wegner RD, Seidel J, Schmidt A, Kuechler A, Schreyer I, Claussen U, Von Eggeling F, Liehr T. Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification. Hum Genet 2003; 114(1): 51-67.
11. Liehr T, Heller A, Starke H, Rubtsov N, Trifonov V, Mrasek K, Weise A, Kuechler A, Claussen U. Microdissection based high resolution multicolor banding for all 24 human chromosomes. Int J Mol Med 2002; 9(4): 335-339.
12. Weise A, Starke H, Heller A, Tonnies H, Volleth M, Stumm M, Senger G, Nietzel A, Claussen U, Liehr T. Chromosome 2 aberrations in clinical cases characterized by high resolution multicolor banding (MCB) and region specific FISH probes. J Med Genet 2002; 39(6): 434-439.
13. Liehr T, Nietzel A, Starke H, Heller A, Weise A, Mrasek K, Claussen U. Characterization of small human marker chromosomes by centromere-specific multicolor-FISH (cenM-FISH) and high resolution multicolor banding (MCB). ECA-newsletter 2002; 10(4): 3-8.
14. Liehr T, Nietzel A, Starke H, Heller A, Weise A, Kuechler A, Senger G, Ebner S, Martin T, Stumm M, Wegner R, Tonnies H, Hoppe C, Claussen U, von Eggeling F. Characterization of small marker chromosomes (SMC) by recently developed molecular cytogenetic approaches. J Ass Genet Techn 2003; 29(2): 5-10.
15. Senger G, Chudoba I, Plesch A. Multicolor?FISH ? the identification of chromosome aberrations by 24 colors. BIOforum 1998; 9(9): 499?503.
16. Heller A, Chudoba I, Bleck C, Senger G, Claussen U, Liehr T. Microdissection based comparative genomic hybridization (micro-CGH) analysis of secondary acute myelogenous leukemias. Int J Oncol 2000; 16(39): 461-468.
17. Starke H, Schreyer I, Kahler C, Fiedler W, Beensen V, Heller A, Nietzel A, Claussen U, Liehr T. Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8. Prenat Diagn 1999; 19(12): 1169-1174.
18. Von Eggeling F, Hoppe C, Bartz U, Starke H, Houge G, Claussen U, Ernst G, Kotzot D, Liehr T. Maternal uniparental disomy 12 in a healthy girl with a 47,XX, +der(12)(:p11gq11:)/ 46,XX karyotype. J Med Genet 2002, 39(7): 519-521.
19. Nietzel A, Heller A, Starke H, Liehr T. Centromere-specific multicolor-FISH (cenM-FISH). In: Rautenstrauss B, Liehr T, eds. FISH-Technology. Berlin: Springer-Labmanual, Springer, 2002; 425-431.
20. Nietzel A, Albrecht B, Starke H, Heller A, Gillessen-Kaesbach G, Claussen U, Liehr T. Partial hexasomy 15pterg15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report. J Med Genet 2003; 40(3), E28: 1-4.
21. Liehr T, Nietzel A, Rocchi M, Heller A, Starke H, Claussen U, von Eggeling F. Centromere-specific multi-color-FISH (cenM-FISH) followed by analysis for uniparental disomy - a useful tool in prenatal diagnosis. In: Macek M, ed. Early Prenatal Diagnosis, Fetal Cells and DNA in the Mother - Present State and Perspectives. Prague: The Karolinum Press, 2002; 293-300.
22. Starke H, Mitulla B, Nietzel A, Heller A, Beensen V, Grosswendt G, Claussen U, von Eggeling F, Liehr T. First case of trisomy 21 accompanied by an additional der(4)(:p11gq11:) plus partial uniparental disomy 4p15-16. Am J Med Genet 2003; 116A(1): 26-30.
23. Starke H, Raida M, Trifonov V, Clement JH, Loncarevic IF, Heller A, Bleck C, Nietzel A, Rubtsov N, Claussen U, Liehr T. Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia. Br J Haematol 2001; 113(2): 435-438.
24. Amor DJ, Choo KH. Neocentromeres: role in human disease, evolution, and centromere study. Am J Hum Genet 2002; 71(4): 695-714.
25. Daniel A, Malafiej P. A Series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15. Am J Med Genet 2003; 117A(3): 212-222.
26. Morison IM, Reeve AE. A catalogue of imprinted genes and parent-of-origin effects in humans and animals. Hum Mol Genet 1998; 7(10): 1599-609.