Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Zierler Hannelore |
Präsentationen bei wissenschaftlichen und nicht-wissenschaftlichen Veranstaltungen
Sodia, S; W. Emberger, H. Zierler, M.Speicher
Prenatal Diagnosis of a fetus with 44 Chromosomes and homozygous translocations (14;21)
European Journal of Human Genetics2008; 16(2):183-183.-European Human Genetics Conference 2008; May 31- June 3,2008; Barcelona , Spain.
[Poster]
Varon, R; Müer, A; Wagner, K; Zierler, H; Sodia, S; Rauter, L; Petek, E; Tönnies, H; Neitzel, H; Sperling, K; Kroisel, PM
Nijmegen breakage syndrome due to maternal isodisomy of chromosome 8.
Medizinische Genetik2006; 18(1):107-107.-GFH, Tagung Halle2006; Mar 8-11, 2006; Halle, GERMANY.
[Poster]
Emberger, W; Regauer, S; Sodial, S; Reich, O; Zierler, H; Wagner, K; Pfragner, R
Endometrial stromal sarcoma: cytogenetic and molecular cytogenetic analyses
EUR J CELL BIOL 2005 84: 17-17.
Web of Science
Emberger, W; Sodia, S; Pfragner, R; Regauer, S; Reich, O; Zierler, H; Petek, E; Wagner, K
Cytogenetic and molecular cytogenetic characterization of an Endometrial Stomal Sarkoma presenting a t(10;17)(q22;p13) translocation.
europ j human genet 2005; 13(1):208-208.-European Human Genetics Conference 2005; MAY 7-10, 2005; Prague, Czech Republic.
[Poster]
Sodia, S; Emberger, W; Zierler, H; Kroisel, PM; Petek, E; Hojas, S; Wagner, K
Cytogenetic and molecular cytogenetic characterisation of t(4;12) involving the ETV6 gene with a novel translocation partner on chromosome 4 in a case of acute myeloid leukaemia.
europ j human genet 2005; 13(1):209-209.-European Human Genetics Conference; MAY 7-10, 2005; Prague, Czech Republic.
[Poster]
Emberger, W; Regauer, S; Windpassinger, C; Petek, E; Sodia, S; Reich, O; Pfragner, R; Zierler, H; Wagner, K
Detection of T439I mutation of BRAF in sinunasal maligant melanoma.
European Human Genetics Conference; 2004.
[Poster]
Emberger, W; Sodia, S; Pfragner, R; Regauer, S; Reich, O; Petek, E; Windpassinger, C; Zierler, H; Kroisel, PM
Cytogenetic Characterization of Vulva-Melanomas.
Medizinische Genetik (medgen). 2003; 15. Jahrgang/ 2003(3):38-38.-Tagung der Deutschen Gesellschaft für Humangenetik (ÖGH); MAY 11 - 14, 2003; GERMANY.
[Poster]
Emberger, W; Sodia, S; Pfragner, R; Regauer, S; Reich, O; Petek, E; Windpassinger, C, Zierler, H, Kroisel, PM; Wagner, K
Cytogenetic Characterization of Vulva-Melanomas.
Medizinische Genetik. 2003; 15. Jahrgang(3):338-338.-14. Jahrestagung der Deutschen Gesellschaft für Humangenetik & mit Österreichische Gesellschaft für Humangenetik & Schweizerische Gesellschaft für Medizinische Genetik. 10. Workshop für Neurogenetik der Deutschen Gesellschaft für Neurogenetik e.V. 16. Tumorzytogenetrische Arbeitstagung; SEP 3, 2003; GERMANY.
[Poster]
Emberger, W; Olipitz, W; Sodia, S; Petek, E; Zierler, H; Kroisel, PM; Wagner, K
Blast crisis in Philadelphia negative CML: Clinical findings and molecular cytogenetic characterization of a 47,XX,+i(11)(q10) cell line.
EUR J HUMAN GENET 2002 10: 105-106.
Web of Science
Kroisel, PM; Windpassinger, C; Zierler, H; Wagner, K; Petek, E
Constitutional microdeletion del(22)(q12.1q12.3) including the NF2 gene region.
EUR J HUMAN GENET 2002 10: 133-133.
Web of Science
Sodia, S; Petek, E; Emberger, W; Zierler, H; Wagener, K; Kroisel, PM
Partial monosomy 13q associated with anophthalmia due to a familial transolcation (9;13)(p24.3;q31.3)
europ j human genet 2001; 9(1):156-157.-10th International congress of Human Genetics; MAY 15-19, 2001; Vienna, Austria.
[Poster]