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 TitleAuthors / EditorsDate
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Impact of cytogenetic abnormalities in adults with Ph-negative B-cell precursor acute lymphoblastic leukemia Lafage-Pochitaloff, Marina; Baranger, Laurence; Hunault, Mathilde; Cuccuini, Wendy; ... Dombret, Hervé 2017
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Fusion genes with ALK as recurrent partner in ependymoma-like gliomas: a new brain tumor entity? Olsen, Thale Kristin; Panagopoulos, Ioannis; Meling, Torstein; Micci, Francesca; ... Brandal, Petter 2015
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Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature Sloan Bena, Frédérique; Bruno, Damien L; Eriksson, Mats; van Ravenswaaij-Arts, Conny; ... Schoumans, Jacqueline 2013
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Network-guided analysis of genes with altered somatic copy number and gene expression reveals pathways commonly perturbed in metastatic melanoma Valsesia, Armand; Rimoldi, Donata; Martinet, Danielle; Ibberson, Mark; ... Stevenson, Brian J 2011
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An effective serum- and xeno-free chemically defined freezing procedure for human embryonic and induced pluripotent stem cells Holm, Frida; Ström, Susanne; Inzunza, José; Baker, Duncan; ... Hovatta, Outi 2010
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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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Immortalized human skin fibroblast feeder cells support growth and maintenance of both human embryonic and induced pluripotent stem cells Unger, Christian; Gao, Shuping; Cohen, Marie-Benoîte; Jaconi, Marisa; ... Feki, Anis 2009
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Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients Martinet, Danielle; Filges, Isabel; Besuchet Schmutz, Nathalie; Morris, Michael Andréw; ... Bena, Frédérique 2008
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Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events Dahoun, Sophie; Gagos, Sarantis; Gagnebin, Maryline; Gehrig, Corinne; ... Blouin, Jean-Louis 2008
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Derivation of the first Swiss human embryonic stem cell line from a single blastomere of an arrested four-cell stage embryo Feki, Anis; Bosman, Alexis; Dubuisson, Jean-Bernard; Irion, Olivier; ... Jaconi, Marisa 2008
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The prognostic significance of cytogenetic aberrations in childhood acute myeloid leukaemia. A study of the Swiss Paediatric Oncology Group (SPOG) Betts, David R; Ammann, Roland A; Hirt, Andreas; Hengartner, Heinz; ... Niggli, Felix K 2007
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Establishment of permanent cell lines purified from human mesothelioma: morphological aspects, new marker expression and karyotypic analysis Philippeaux, Marie-Marthe; Pache, Jean-Claude; Dahoun, Sophie; Barnet, Marc; ... Spiliopoulos, Anastase 2004
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Lentivector-mediated transfer of Bmi-1 and telomerase in muscle satellite cells yields a Duchenne myoblast cell line with long-term genotypic and phenotypic stability Cudré-Mauroux, Christophe; Occhiodoro, Teresa; Konig, Stéphane; Salmon, Patrick; ... Trono, Didier 2003
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Pregnancy outcome of 30 fetuses with cystic hygroma diagnosed during the first 15 weeks of gestation Giacobino, Ariane; Extermann, D; Extermann, Ph; Dahoun, Sophie 2003
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Genomic structure of a copy of the human TPTE gene which encompasses 87 kb on the short arm of chromosome 21 Guipponi, Michel; Yaspo, M. L.; Riesselman, L.; Chen, H.; ... Antonarakis, Stylianos 2000
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A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonography Giacobino, Ariane; Dahoun, Sophie; Sizonenko, Pierre-Claude; Stalberg, Anna-Maria; ... Campana, Aldo 2000
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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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Wilms' tumor in the adult--report of a case and review of the literature Tawil, A; Cox, J N; Roth, Arnaud; Briner, J; ... Remadi, Sami 1999
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Increased levels of a chromosome 21-encoded tumour invasion and metastasis factor (TIAM1) mRNA in bone marrow of Down syndrome children during the acute phase of AML(M7) Ives, J. H.; Dagna-Bricarelli, F.; Basso, G.; Antonarakis, Stylianos; ... Nizetic, D. 1998
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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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