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文章名     作者     期刊名     摘要     卷     期         如果没有找到您所需要的文献，请点击 ——此处申请     共10条记录   Coamplification of Multiple Regions of Chromosome 2, Including MYCN, in a Single Patchwork Amplicon in Cancer Cell Lines [作者：Kitada, K; Aida, S; Aikawa, S,期刊：Cytogenetic and Genome Research, 页码：30-37 , 文章类型： Article，,卷期：2012年136-1] Coamplification of multiple segments of chromosome 2, including an MYCN-bearing segment, was examined in 2 cancer cell lines, NCI-H69 (lung cancer) and IMR-32 (neuroblastoma). High-resolution array-CGH analysis revealed ... SNP Analysis of Minimally Evolved t(14;18) (q32;q21)-Positive Follicular Lymphomas Reveals a Common Copy-Neutral Loss of Heterozygosity Pattern [作者：Cheung, KJ; Rogic, S; Ben-Neriah, S; Boyle, M; Connors, JM; Gascoyne, RD; Horsman, DE,期刊：Cytogenetic and Genome Research, 页码：38-43 , 文章类型： Article，,卷期：2012年136-1] Follicular lymphoma (FL) cases with a t(14;18)(q32;q21) and minimal or no additional karyotypic alterations, such as copy number gains and losses and/or chromosomal rearrangements, may exhibit pathologic features and a c... Molecular Cytogenetic Aberrations in Tunisian Patients with Multiple Myeloma Identified by cIg-FISH in Fixed Bone Marrow Cells [作者：Gmidene, A; Avet-Loiseau, H; Sennana, H; Ben Abdallah, I; Khlif, A; Meddeb, B; Elloumi, M; Saad, A,期刊：Cytogenetic and Genome Research, 页码：44-49 , 文章类型： Article，,卷期：2012年136-1] Cytogenetic studies in multiple myeloma (MM) are hampered by the hypo-proliferative nature of plasma cells. In order to circumvent this problem, we have used a combination of immunolabeling of cytoplasmic Ig light chains... The Expression of Preaxial Polydactyly Is Influenced by Modifying Genetic Elements and Is Not Maintained by Chromosomal Inversion in an Avian Biomedical Model [作者：Robb, EA; Delany, ME,期刊：Cytogenetic and Genome Research, 页码：50-68 , 文章类型： Article，,卷期：2012年136-1] Polydactyly (Po) is a common mutation found in many vertebrates. The UCD-Po.003 congenic chicken line was previously characterized for Po inheritance (autosomal dominant) and the mutation was mapped to chromosome 2p. Her... The Sockeye Salmon Neo-Y Chromosome Is a Fusion between Linkage Groups Orthologous to the Coho Y Chromosome and the Long Arm of Rainbow Trout Chromosome 2 [作者：Faber-Hammond, J; Phillips, RB; Park, LK,期刊：Cytogenetic and Genome Research, 页码：69-74 , 文章类型： Article，,卷期：2012年136-1] Unlike other Pacific salmon, sockeye salmon (Oncorhynchus nerka) have an X1X2Y sex chromosome system, with females having a diploid chromosome number of 2n = 58 and males 2n = 57 in all populations examined. To determine... Cryptic Introgression of Dasypyrum villosum Parental DNA in Wheat Lines Derived from Intergeneric Hybridization [作者：Caceres, ME; Pupilli, F; Ceccarelli, M; Vaccino, P; Sarri, V; De Pace, C; Cionini, PG,期刊：Cytogenetic and Genome Research, 页码：75-81 , 文章类型： Article，,卷期：2012年136-1] Cytogenetic and DNA molecular analyses have been carried out in 3 wheat introgression lines (ILs; CS x V58, CS x V59, and CS x V60) derived from Triticum aestivum cv. 'Chinese Spring' (CS) x Dasypyrum villosum (Dv) inter... A New Case of Pure Partial 7q Duplication [作者：Alfonsi, M; Palka, C; Morizio, E; Gatta, V; Franchi, S; Franchi, PG; Zori, R; Calabrese, G; Palka, G; Chiarelli, F,期刊：Cytogenetic and Genome Research, 页码：1-5 , 文章类型： Article，,卷期：2012年136-1] We report on an 18-month-old boy conceived by assisted reproduction technology with developmental delay, hypotonia, microcephaly, frontal bossing, a mild convergent squint, malformed ears, and a short neck. Karyotype ana... Characterizing Small Supernumerary Marker Chromosomes with Combination of Multiple Techniques [作者：Yu, S; Fiedler, SD; Brawner, SJ; Joyce, JM; Zhou, XG; Liu, HY,期刊：Cytogenetic and Genome Research, 页码：6-14 , 文章类型： Article，,卷期：2012年136-1] Fourteen cases with constitutional small supernumerary marker chromosomes (sSMCs) were assessed by combination of diverse techniques including genome-wide high-resolution chromosomal microarray (CMA), chromosome banding ... Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing [作者：Vlckova, M; Trkova, M; Zemanova, Z; Hancarova, M; Novotna, D; Raskova, D; Puchmajerova, A; Drabova, J; Zmitkova, Z; Tan, Y; Sedlacek, Z,期刊：Cytogenetic and Genome Research, 页码：15-20 , 文章类型： Article，,卷期：2012年136-1] Proximal 6q deletions have a milder phenotype than middle and distal 6q deletions. We describe 2 patients with non-overlapping deletions of about 15 and 19 Mb, respectively, which subdivide the proximal 6q region into 2 ... Chromosome Breakage in Human Preimplantation Embryos from Carriers of Structural Chromosomal Abnormalities in Relation to Fragile Sites, Maternal Age, and Poor Sperm Factors [作者：Xanthopoulou, L; Ghevaria, H; Mantzouratou, A; Serhal, P; Doshi, A; Delhanty, JDA,期刊：Cytogenetic and Genome Research, 页码：21-29 , 文章类型： Article，,卷期：2012年136-1] Chromosome breakage is a fairly widespread phenomenon in preimplantation embryos affecting at least 10% of day 3 cleavage stage embryos. It may be detected during preimplantation genetic diagnosis (PGD). For carriers of ...