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A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24 de Mollerat, X. J.; Gurrieri, Fiorella; Morgan, C. T.; Sangiorgi, Eugenio; ... Schwartz, C. E. 2003
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BACking up the promises Antonarakis, Stylianos 2001
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BDNF and DYRK1A are variable and inversely correlated in lymphoblastoid cell lines from Down syndrome patients Tlili, Asma; Hoischen, Alexander; Ripoll, Clémentine; Benabou, Eva; ... Janel, Nathalie 2012
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Chromosome 21: a small land of fascinating disorders with unknown pathophysiology Antonarakis, Stylianos; Lyle, Robert; Deutsch, Samuel; Reymond, Alexandre 2002
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Comparison of microsatellite instability and chromosomal instability in predicting survival of patients with T3N0 colorectal cancer Gervaz, Pascal; Cerottini, Jean-Philippe; Bouzourene, Hanifa; Hahnloser, Dieter; ... Carethers, John M 2002
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Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia Rogan, P. K.; Close, P.; Blouin, Jean-Louis; Seip, J. R.; ... Antonarakis, Stylianos 1995
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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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Fusion genes with ALK as recurrent partner in ependymoma-like gliomas: a new brain tumor entity? Olsen, Thale Kristin; Panagopoulos, Ioannis; Meling, Torstein R; Micci, Francesca; ... Brandal, Petter 2015
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High incidence of ectopic nucleolar organizer regions in human testicular tumors Neerman Arbez, Marguerite; Delozier-Blanchet, C. D.; Bolle, J. F.; Rondez, R.; Morris, Michael Andréw 1993
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Impaired activation of face processing networks revealed by functional magnetic resonance imaging in 22q11.2 deletion syndrome Andersson, Frédéric; Glaser, Bronwyn; Spiridon Paltani, Mona; Debbané, Martin; ... Eliez, Stéphan 2008
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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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Normal phenotype with paternal uniparental isodisomy for chromosome 21 Blouin, Jean-Louis; Avramopoulos, D.; Pangalos, C.; Antonarakis, Stylianos 1993
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Pericentromeric instability and spontaneous emergence of human neoacrocentric and minute chromosomes in the alternative pathway of telomere lengthening Gagos, Sarantis; Chiourea, Maria; Christodoulidou, Agni; Apostolou, Eftichia; ... Antonarakis, Stylianos 2008
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Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes Mefford, H. C. 2008
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The Glanville fritillary genome retains an ancient karyotype and reveals selective chromosomal fusions in Lepidoptera Lehtonen, Rainer; Waterhouse, Robert; Holm, Liisa; Auvinen, Petri; Frilander, Mikko J 2014
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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