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Number of items: 7.

Begemann, M; Spengler, S; Kanber, D; Haake, A; Baudis, M; Leisten, I; Binder, G; Markus, S; Rupprecht, T; Segerer, H; Fricke-Otto, S; Mühlenberg, R; Siebert, R; Buiting, K; Eggermann, T (2011). Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues. Clinical Genetics, 80(1):83-88.

Eggermann, T; Spengler, S; Bachmann, N; Baudis, M; Mau-Holzmann, U A; Singer, S; Rossier, E (2010). Chromosome 11p15 duplication in Silver-Russell syndrome due to a maternally inherited translocation t(11;15). American Journal of Medical Genetics. Part A, 152A(6):1484-1487.

Eggermann, T; Schönherr, N; Spengler, S; Jäger, S; Denecke, B; Binder, G; Baudis, M (2010). Identification of a 21q22 duplication in a Silver-Russell syndrome patient further narrows down the Down syndrome critical region. American Journal of Medical Genetics. Part A, 152A(2):356-359.

Spengler, S; Schönherr, N; Binder, G; Wollmann, H; Fricke-Otto, S; Mühlenberg, R; Denecke, B; Baudis, M; Eggermann, T (2010). Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome. Journal of Medical Genetics, 47(5):356-360.

Muetze, S; Eggermann, T; Leeners, B; Birke, C; Kuse, S; Ortlepp, J R; Rudnik-Schoeneborn, S; Zerres, K; Rath, W (2009). The 4G/5G polymorphism in the plasminogen activator inhibitor-1 gene is not associated with HELLP syndrome. Journal of Thrombosis and Thrombolysis, 27(2):141-145.

Roos, A; Elbracht, M; Baudis, M; Senderek, J; Schönherr, N; Eggermann, T; Schüler, H M (2008). A 10.7 Mb interstitial deletion of 13q21 without phenotypic effect defines a further non-pathogenic euchromatic variant. American Journal of Medical Genetics. Part A, 146A(18):2417-2420.

Wiesmüller, G A; Weissbach, W; Mommers, M; Weishoff-Houben, M; Dott, W; Karaahmetoglu, Y; Kunert, H J; Podoll, K; Hoff, P; Blömeke, B; Merk, H F; Setani, K; Büll, U; Ilgner, J; Westhofen, M; Ortlepp, J R; Hanrath, P; Zerres, K; Eggermann, T (2003). Einflüsse von genetischen Prädispositionen und Umweltfaktoren auf Erkrankungen des Menschen. Arbeitsmedizin, Sozialmedizin, Umweltmedizin, 38(10):522-527.

This list was generated on Sun Jun 24 09:48:14 2018 CEST.