A STRATEGY FOR THE CHARACTERIZATION OF SMALL SUPERNUMERARY MARKER CHROMOSOMES (SMC)
Liehr T*, Nietzel A, Weise A, Mrasek K, von Eggeling F, Claussen U, Starke H
*Corresponding Author: Dr. Thomas Liehr, Institut für Humangenetik, Postfach, D-07740 Jena, Germany; Tel: +49-3641-935533; Fax. +49-3641-935502; E-mail: i8lith@mti.uni-jena.de
page: 69

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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.

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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.

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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.

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