Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Präsentationen bei wissenschaftlichen und nicht-wissenschaftlichen Veranstaltungen

Roetzer, KM; Obenauf, AC; Schwarzbraun, T; Uhrig, S; Emberger, W; Sodia, S; Mach, M; Vallant, E; Hauser, E; Wagner, K; Kroisel, PM; Speicher, MR Array-CGH for the identification of constitutional copy number changes
DECIPHER Symposium; MAY 19-21, 2010; Cambridge, GREAT BRITAIN. 2010. [Oral Communication]

 

Fiegl, M; Erdel, M; Tinhofer, I; Hopfinger, G; Eigenberger, K; Falkner, F; Falkner, A; Brychtova, Y; Panovska, A; Doubek, M; Zabernigg, A; Sodia, S; Muhlberger, H; Gastl, G; Mayer, J; Greil, R Clinical Outcome of B-Cell Chronic Lymphocytic Leukemia Following Alemtuzumab Therapy: Retrospective Study within Various Cytogenetic Risk Categories
BLOOD. 2008; 112(11): 1085-1085. [Poster]
Web of Science

 

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]

 

Juch, H; Sodia, S; Emberger, W; Dohr, G; Teratologic Aspects of Assisted Reproductive Technologies.
The annual ENTIS-meeting; JUN 8-10, 2007; Helsinki FINNLAND. 2007. [Oral Communication]

 

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]

 

Pfragner, R; Emberger, W; Sodia, S; Reich, S; Regauer, S Human mucosa-associated malignant melanomas: cytogenetic and molecular genetic characterizatiohn.
Fall Meeting of the Society for Biochemistry and Molecular Biology, 45th International Meeting of the European Tissue Culture Socierty (ETCS) and the Annual Meeting of the German Society for Cell and Tissue Culture (Deutsche Gesellschaft für Zell- und Gewebezüchtung (GZG); SEP 19 - 22, 2004; Münster, GERMANY. 2004. [Keynote lecture]

 

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

 

Sodia, S; Emberger, W; Rauter, L; Petek, E; Zierler, H; Wagner, K; Kroisel, PM Constitutional mosaicism for a partial trisomy 8 in a patient with a Chromosome Breakage Syndrome
EUR J HUMAN GENET 2002 10: 130-130.
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]

 

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