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 TitleAuthors / EditorsDate
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Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy Rudolf, Gabrielle; Lesca, Gaetan; Fluss, Joel Victor; Abbas, Mohamed 2016
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A t(17;22)(q21;q12) with partial ETV4 deletion in a soft tissue Ewing sarcoma Rougemont-Pidoux, Anne-Laure; Bouron-Dal Soglio, Dorothée; Patey-Mariaud de Serre, Natacha; Fetni, Raouf; ... Fournet, Jean-Christophe 2012
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Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1 Cironi, Luisa; Provero, Paolo; Riggi, Nicola; Janiszewska, Michalina; ... Stamenkovic, Ivan 2009
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The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminoma Gimelli, Stefania; Beri, Silvana; Drabkin, Harry A.; Gambini, Claudio; ... Gimelli, Giorgio 2009
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Non-classical karyotypic features in relapsed childhood B-cell precursor acute lymphoblastic leukemia Wehrli, Lea A.; Braun, Julia; Buetti, Luisa Nobile; Hagleitner, Nicole; ... Bourquin, Jean-Pierre 2009
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Evidence for genes in addition to Tlr7 in the Yaa translocation linked with acceleration of systemic lupus erythematosus Santiago-Raber, Marie-Laure; Kikuchi, Shuichi; Borel, Paula; Uematsu, Satoshi; ... Izui, Shozo 2008
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PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse Peeters, H; Debeer, P; Bairoch, Amos Marc; Wilquet, V; ... Devriendt, Koenraad 2003
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A t(2;8) balanced translocation with breakpoints near the human HOXD complex causes mesomelic dysplasia and vertebral defects Spitz, François; Montavon, Thomas; Monso-Hinard, Christine; Morris, Michael Andréw; ... Duboule, Denis 2002
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Trisomy 1q generating translocations in Wilms tumor Betts, D R; Ilg, E C; Ozsahin, Ayse Hulya; von der Weid, N; Niggli, F K 1999
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Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13 Eliez, Stéphan; Morris, Michael Andréw; Dahoun-Hadorn, S.; DeLozier-Blanchet, C. D.; ... Antonarakis, Stylianos 1997
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Fortuitous detection of uniparental isodisomy of chromosome 6 Bittencourt, M. C.; Morris, Michael Andréw; Chabod, J.; Gos, A.; ... Tiberghien, P. 1997
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YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome Nadal, M.; Mila, M.; Pritchard, M.; Mur, A.; ... Estivill, X. 1996
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Biparental inheritance of chromosome 21 polymorphic markers indicates that some Robertsonian translocations t(21;21) occur postzygotically Blouin, Jean-Louis; Binkert, F.; Antonarakis, Stylianos 1994
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Biology and facultative secretion of plasminogen activator inhibitor-2 Belin, Dominique 1993