Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification von Starke, Heike, Nietzel, Angela, Weise, Anja, Heller, Anita, Mrasek, Kristin, Belitz, Britta, Kelbova, Christine, Volleth, Marianne, Albrecht, Beate, Mitulla, Beate, Trappe, Ralf, Bartels, Iris, Adolph, Sabine, Dufke, Andreas, Singer, Sylke, Stumm, Markus, Wegner, Rolf-Dieter, Seidel, Jörg, Schmidt, Angela, Kuechler, Alma, Schreyer, Isolde, Claussen, Uwe, von Eggeling, Ferdinand, Liehr, Thomas

Volltext

Parental Origin and Timing of De Novo Robertsonian Translocation Formation von Bandyopadhyay, Ruma, Heller, Anita, Knox-DuBois, Cami, McCaskill, Christopher, Berend, Sue Ann, Page, Scott L., Shaffer, Lisa G.

Volltext

Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells von Erlecke, Jörn, Hartmann, Isabell, Hoffmann, Martin, Kroll, Torsten, Starke, Heike, Heller, Anita, Gloria, Alexander, Sayer, Herbert G, Johannes, Tilman, Claussen, Uwe, Liehr, Thomas, Loncarevic, Ivan F

Volltext

Clinical impact of nucleophosmin mutations and Flt3 internal tandem duplications in patients older than 60 yr with acute myeloid leukaemia von Scholl, Sebastian, Theuer, Claudia, Scheble, Veit, Kunert, Christa, Heller, Anita, Mügge, Lars-Olof, Fricke, Hans-Joerg, Höffken, Klaus, Wedding, Ulrich

Volltext

A new multicolor-FISH approach for the characterization of marker chromosomes : Centromere-specific multicolor-FISH (CenM-FISH) von NIETZEL, Angela, ROCCHI, Mariano, STARKE, Heike, HELLER, Anita, FIEDLER, Wolfgang, WLODARSKA, Iwona, LONCAREVIC, Ivan F, BEENSEN, Volkmar, CLAUSSEN, Uwe, LIEHR, Thomas

Volltext

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements von Starke, Heike, Seidel, Jörg, Henn, Wolfram, Reichardt, Sylvia, Volleth, Marianne, Stumm, Markus, Behrend, Christine, Sandig, Klaus R, Kelbova, Christine, Senger, Gabriele, Albrecht, Beate, Hansmann, Ingo, Heller, Anita, Claussen, Uwe, Liehr, Thomas

Volltext

Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype von GROSS, Madeleine, MKRTCHYAN, Hasmik, GLASER, Melanie, FRICKE, Hans Jörg, HÖFFKEN, Klaus, HELLER, Anita, WEISE, Anja, LIEHR, Thomas

Volltext

Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics von Manvelyan, Marina, Kempf, Philipp, Weise, Anja, Mrasek, Kristin, Heller, Anita, Lier, Amelie, Höffken, Klaus, Fricke, Hans-Jörg, Sayer, Herbert, Liehr, Thomas, Mkrtchyan, Hasmik

Volltext

FISH banding methods: applications in research and diagnostics von Liehr, Thomas, Heller, Anita, Starke, Heike, Claussen, Uwe

Volltext

Karyotyping of human synaptonemal complexes by cenM-FISH von OLIVER-BONET, Maria, LIEHR, Thomas, NAVARRO, Joaquima, BENET, Jordi, NIETZEL, Angela, HELLER, Anita, STARKE, Heike, CLAUSSEN, Uwe, CODINA-PASCUAL, Montserrat, PUJOL, Aïda, ABAD, Carlos, EGOZCUE, Josep

Volltext

Genotype/phenotype analysis in a patient with pure and complete trisomy 12p von Zumkeller, Walter, Volleth, Marianne, Muschke, Petra, Tönnies, Holger, Heller, Anita, Liehr, Thomas, Wieacker, Peter, Stumm, Markus

Volltext

Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter von Trifonov, Vladimir, Seidel, Jörg, Starke, Heike, Martina, Prechtel, Beensen, Volkmar, Ziegler, Monika, Hartmann, Isabell, Heller, Anita, Nietzel, Angela, Claussen, Uwe, Liehr, Thomas

Volltext

Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review von Heller, Anita, Seidel, J, Hübler, A, Starke, H, Beensen, V, Senger, G, Rocchi, M, Wirth, J, Chudoba, I, Claussen, U, Liehr, T

Volltext

Tapping an unexploited repository: Carnoy's fixed cell pellets for proteomic biomarker research in leukemia von Von Eggeling, Ferdinand, Bleul, Annett, Loncarevic, Ivan F, Michel, Susanne, Heller, Anita, Melle, Christian

Volltext

Genetic imbalances in 26 cases of penile squamous cell carcinoma von Alves, Gilda, Heller, Anita, Fiedler, Wolfgang, Campos, Mércia Mendes, Claussen, Uwe, Ornellas, Antônio Augusto, Liehr, Thomas

Volltext

Small supernumerary marker chromosomes von Starke, Heike, Nietzel, Angela, Weise, Anja, Heller, Anita, Mrasek, Kristin, Belitz, Britta, Kelbova, Christine

Volltext

Dup(13)(q14.2-q14.3): Yet Another New Differential Diagnostic Aspect for Short Stature-like Phenotype von Schreyer, Isolde, Neumann, Annett, Beensen, Volkmar, Eichhorn, Karl-Heinz, Heller, Anita, Claussen, Uwe, Liehr, Thomas

Volltext

Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2) von Liehr, Thomas, Heller, Anita, Eichhorn, Karl-Heinz, Beensen, Volkmar, Schulze, Eberhart, Starke, Heike, Claussen, Uwe, Schreyer, Isolde

Volltext

Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia‐negativ... von Starke, Heike, Raida, Martin, Trifonov, Vladimir, Clement, Joachim H., Loncarevic, Ivan F., Heller, Anita, Bleck, Cordula, Nietzel, Angela, Rubtsov, Nikolai, Claussen, Uwe, Liehr, Thomas

Volltext

First patient with trisomy 21 accompanied by an additional der(4)(:p11 → q11:) plus partial uniparental disomy 4p15-16 von Starke, Heike, Mitulla, Beate, Nietzel, Angela, Heller, Anita, Beensen, Volkmar, Grosswendt, Gisela, Claussen, Uwe, von Eggeling, Ferdinand, Liehr, Thomas

Volltext