
Vol. 118, No. 1, 2007 September 2007
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Original Article
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1
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Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation
Thuresson, A.-C. ;
Bondeson, M.-L. ;
Edeby, C. ;
Ellis, P. ;
Langford, C. ;
Dumanski, J.P. ;
Annerén, G.
Cytogenet Genome Res 2007;118:1-7 (DOI:10.1159/000106434)
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Article (PDF 264 KB)
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8
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High-resolution oligonucleotide array-CGH pinpoints genes involved in cryptic losses in chronic lymphocytic leukemia
Tyybäkinoja, A. ;
Vilpo, J. ;
Knuutila, S.
Cytogenet Genome Res 2007;118:8-12 (DOI:10.1159/000106435)
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Article (PDF 390 KB)
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13
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Tiling resolution array CGH of dic(7;9)(p11~13;p11~13) in B-cell precursor acute lymphoblastic leukemia reveals clustered breakpoints at 7p11.2~12.1 and 9p13.1
Lundin, C. ;
Heidenblad, M. ;
Strömbeck, B. ;
Borg, Å. ;
Hovland, R. ;
Heim, S. ;
Johansson, B.
Cytogenet Genome Res 2007;118:13-18 (DOI:10.1159/000106436)
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Article (PDF 625 KB)
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19
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Variation of CNV distribution in five different ethnic populations
White, S.J. ;
Vissers, L.E.L.M. ;
Geurts van Kessel, A. ;
de Menezes, R.X. ;
Kalay, E. ;
Lehesjoki, A.E. ;
Giordano, P.C. ;
van de Vosse, E. ;
Breuning, M.H. ;
Brunner, H.G. ;
den Dunnen, J.T. ;
Veltman, J.A.
Cytogenet Genome Res 2007;118:19-30 (DOI:10.1159/000106437)
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Article (PDF 602 KB)
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31
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Neocentric small supernumerary marker chromosomes (sSMC) - three more cases and review of the literature
Liehr, T. ;
Utine, G.E. ;
Trautmann, U. ;
Rauch, A. ;
Kuechler, A. ;
Pietracz, J. ;
Bocian, E. ;
Kosyakova, N. ;
Mrasek, K. ;
Boduroglu, K. ;
Weise, A. ;
Aktas, D.
Cytogenet Genome Res 2007;118:31-37 (DOI:10.1159/000106438)
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Article (PDF 476 KB)
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38
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Initial maternal meiotic I error leading to the formation of a maternal i(2q) and a paternal i(2p) in a healthy male
Baumer, A. ;
Basaran, S. ;
Taralczak, M. ;
Cefle, K. ;
Ozturk, S. ;
Palanduz, S. ;
Schinzel, A.
Cytogenet Genome Res 2007;118:38-41 (DOI:10.1159/000106439)
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42
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Human chromosome 1 satellite 3 DNA is decondensed, demethylated and transcribed in senescent cells and in A431 epithelial carcinoma cells
Enukashvily, N.I. ;
Donev, R. ;
Waisertreiger, I.S.-R. ;
Podgornaya, O.I.
Cytogenet Genome Res 2007;118:42-54 (DOI:10.1159/000106440)
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55
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Sequence analysis of the equine SLC26A2 gene locus on chromosome 14q15 q21
Hansen, M. ;
Knorr, C. ;
Hall, A.J. ;
Broad, T.E. ;
Brenig, B.
Cytogenet Genome Res 2007;118:55-62 (DOI:10.1159/000106441)
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Article (PDF 297 KB)
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63
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Cytogenetic mapping of eight genes encoding fatty acid binding proteins (FABPs) in the pig genome
Szczerbal, I. ;
Chmurzynska, A. ;
Switonski, M.
Cytogenet Genome Res 2007;118:63-66 (DOI:10.1159/000106442)
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67
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Exclusion of NFYB as candidate gene for congenital splay leg in piglets and radiation hybrid mapping of further five homologous porcine genes from human chromosome 12 (HSA12)
Boettcher, D. ;
Paul, S. ;
Bennewitz, J. ;
Swalve, H.H. ;
Thaller, G. ;
Maak, S.
Cytogenet Genome Res 2007;118:67-71 (DOI:10.1159/000106443)
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Free Supplement Material (42 KB)
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72
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Karyotypic differences in two sibling species of Scotophilus from South Africa (Vespertilionidae, Chiroptera, Mammalia)
Eick, G.N. ;
Jacobs, D.S. ;
Yang, F. ;
Volleth, M.
Cytogenet Genome Res 2007;118:72-77 (DOI:10.1159/000106444)
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78
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Comparative chromosome mapping of 5S rDNA and 5SHindIII repetitive sequences in Erythrinidae fishes (Characiformes) with emphasis on the Hoplias malabaricus 'species complex'
Ferreira, I.A. ;
Bertollo, L.A.C. ;
Martins, C.
Cytogenet Genome Res 2007;118:78-83 (DOI:10.1159/000106445)
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Human Cytogenetics Case Report
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84
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Duplication dup(1)(q41q44) defined by fluorescence in situ hybridization: delineation of the 'trisomy 1q42 qter syndrome'
Coccé, M.C. ;
Villa, O. ;
Obregon, M.G. ;
Salido, M. ;
Barreiro, C. ;
Solé, F. ;
Gallego, M.S.
Cytogenet Genome Res 2007;118:84-86 (DOI:10.1159/000106446)
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