A new multicolor-FISH approach for the characterization of marker chromosomes : Centromere-specific multicolor-FISH (CenM-FISH)
NIETZEL, Angela, ROCCHI, Mariano, STARKE, Heike, HELLER, Anita, FIEDLER, Wolfgang, WLODARSKA, Iwona, LONCAREVIC, Ivan F, BEENSEN, Volkmar, CLAUSSEN, Uwe, LIEHR, Thomas
Published in Human genetics (01.03.2001)
Published in Human genetics (01.03.2001)
Get full text
Journal Article
Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter
Trifonov, Vladimir, Seidel, Jörg, Starke, Heike, Martina, Prechtel, Beensen, Volkmar, Ziegler, Monika, Hartmann, Isabell, Heller, Anita, Nietzel, Angela, Claussen, Uwe, Liehr, Thomas
Published in Prenatal diagnosis (01.05.2003)
Published in Prenatal diagnosis (01.05.2003)
Get full text
Journal Article
Dup(13)(q14.2-q14.3): Yet Another New Differential Diagnostic Aspect for Short Stature-like Phenotype
Schreyer, Isolde, Neumann, Annett, Beensen, Volkmar, Eichhorn, Karl-Heinz, Heller, Anita, Claussen, Uwe, Liehr, Thomas
Published in The journal of histochemistry and cytochemistry (01.03.2005)
Published in The journal of histochemistry and cytochemistry (01.03.2005)
Get full text
Journal Article
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)
Liehr, Thomas, Heller, Anita, Eichhorn, Karl-Heinz, Beensen, Volkmar, Schulze, Eberhart, Starke, Heike, Claussen, Uwe, Schreyer, Isolde
Published in Prenatal diagnosis (15.12.2004)
Published in Prenatal diagnosis (15.12.2004)
Get full text
Journal Article
Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases
Kinne, R W, Liehr, T, Beensen, V, Kunisch, E, Zimmermann, T, Holland, H, Pfeiffer, R, Stahl, H D, Lungershausen, W, Hein, G, Roth, A, Emmrich, F, Claussen, U, Froster, U G
Published in Arthritis research (01.01.2001)
Published in Arthritis research (01.01.2001)
Get full text
Journal Article
Synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis and other inflammatory joint diseases show chromosomal aberrations
Kinne, Raimund W., Kunisch, Elke, Beensen, Volkmar, Zimmermann, Thomas, Emmrich, Frank, Petrow, Peter, Lungershausen, Wolfgang, Hein, Gert, Braun, Rudolf K., Foerster, Martin, Kroegel, Claus, Winter, Rando, Liesaus, Eckehard, Fuhrmann, Renée A., Roth, Andreas, Claussen, Uwe, Liehr, Thomas
Published in Genes chromosomes & cancer (01.09.2003)
Published in Genes chromosomes & cancer (01.09.2003)
Get full text
Journal Article
First patient with trisomy 21 accompanied by an additional der(4)(:p11 → q11:) plus partial uniparental disomy 4p15-16
Starke, Heike, Mitulla, Beate, Nietzel, Angela, Heller, Anita, Beensen, Volkmar, Grosswendt, Gisela, Claussen, Uwe, von Eggeling, Ferdinand, Liehr, Thomas
Published in American journal of medical genetics. Part A (01.01.2003)
Published in American journal of medical genetics. Part A (01.01.2003)
Get full text
Journal Article
Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei
Liehr, Thomas, Schreyer, Isolde, Neumann, Annett, Beensen, Volkmar, Ziegler, Monika, Hartmann, Isabell, Starke, Heike, Heller, Anita, Nietzel, Angela, Claussen, Uwe
Published in Prenatal diagnosis (01.06.2002)
Published in Prenatal diagnosis (01.06.2002)
Get full text
Journal Article
First postnatal case of mosaic del(22)/r(22)
Starke, Heike, Mitulla, Beate, Beensen, Volkmar, Trifonov, Vladimir, Rubtsov, Nikolai, Heller, Anita, Ziegler, Monika, Neumann, Annett, Claussen, Uwe, Liehr, Thomas
Published in Prenatal diagnosis (01.09.2003)
Published in Prenatal diagnosis (01.09.2003)
Get full text
Journal Article
Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting
Rubtsov, N, Senger, G, Kuzcera, H, Neumann, A, Kelbova, C, Junker, K, Beensen, V, Claussen, U
Published in Human genetics (01.06.1996)
Published in Human genetics (01.06.1996)
Get more information
Journal Article
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature
SEIDEL, Jörg, HELLER, Anita, ZINTL, Felix, CLAUSSEN, Uwe, LIEHR, Thomas, SENGER, Gabriele, STARKE, Heike, CHUDOBA, Ilse, KELBOVA, Christina, TÖNNIES, Holger, NEITZEL, Heidemarie, HAASE, Claudia, BEENSEN, Volkmar
Published in European journal of pediatrics (01.09.2003)
Published in European journal of pediatrics (01.09.2003)
Get full text
Journal Article
Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8
Starke, Heike, Schreyer, Isolde, Kähler, Christine, Fiedler, Wolfgang, Beensen, Volkmar, Heller, Anita, Nietzel, Angela, Claussen, Uwe, Liehr, Thomas
Published in Prenatal diagnosis (01.12.1999)
Published in Prenatal diagnosis (01.12.1999)
Get full text
Journal Article
Pitfalls of rapid prenatal diagnosis using the interphase nucleus
Liehr, Thomas, Beensen, Volkmar, Hauschild, Rüdiger, Ziegler, Monika, Hartmann, Isabell, Starke, Heike, Heller, Anita, Kähler, Christine, Schmidt, Matthias, Reiber, Wolfgang, Hesse, Martin, Claussen, Uwe
Published in Prenatal diagnosis (01.05.2001)
Published in Prenatal diagnosis (01.05.2001)
Get full text
Journal Article
Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH
Liehr, T, Starke, H, Beensen, V, Kähler, C, Harbich, M, Brude, E, Ziegler, M, Claussen, U
Published in International journal of molecular medicine (01.01.1999)
Published in International journal of molecular medicine (01.01.1999)
Get more information
Journal Article
Insulin-like Growth Factor Serum Concentrations Reflect Insufficient Growth in a Hypoplastic Infant with Partial Trisomy 9q in the 12th Week of Life
Hiibler, A., Seidel, J., Kauf, Ε., Schramm, D., Beensen, V., Heller, A., Liehr, T., Zintl, F.
Published in Journal of Pediatric Endocrinology and Metabolism (2000)
Published in Journal of Pediatric Endocrinology and Metabolism (2000)
Get full text
Journal Article
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)
Liehr, Thomas, Heller, Anita, Eichhorn, Karl-Heinz, Beensen, Volkmar, Schulze, Eberhart, Starke, Heike, Claussen, Uwe, Schreyer, Isolde
Published in Prenatal diagnosis (15.12.2004)
Get full text
Published in Prenatal diagnosis (15.12.2004)
Report
Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei
Liehr, Thomas, Schreyer, Isolde, Neumann, Annett, Beensen, Volkmar, Ziegler, Monika, Hartmann, Isabell, Starke, Heike, Heller, Anita, Nietzel, Angela, Claussen, Uwe
Published in Prenatal diagnosis (01.06.2002)
Get full text
Published in Prenatal diagnosis (01.06.2002)
Report
Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter
Trifonov, Vladimir, Seidel, Jörg, Starke, Heike, Martina, Prechtel, Beensen, Volkmar, Ziegler, Monika, Hartmann, Isabell, Heller, Anita, Nietzel, Angela, Claussen, Uwe, Liehr, Thomas
Published in Prenatal diagnosis (01.05.2003)
Get full text
Published in Prenatal diagnosis (01.05.2003)
Report