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                             57 results found
no title author magazine year volume issue page(s) type
1 Aberrant methylation of the TERT promoter in esophageal squamous cell carcinoma Deng, Jiaying
2015
258-259 12 p. 602-609
8 p.
article
2 Analysis of genomic alterations in neuroblastoma by multiplex ligation-dependent probe amplification and array comparative genomic hybridization: a comparison of results Combaret, Valérie
2012
258-259 12 p. 657-664
8 p.
article
3 A novel TCF3-HLF fusion transcript in acute lymphoblastic leukemia with a t(17;19)(q22;p13) Panagopoulos, Ioannis
2012
258-259 12 p. 669-672
4 p.
article
4 A possible 5′-NRIP1/UHRF1-3′ fusion gene detected by array CGH analysis in a Ph+ ALL patient Zhang, Rui
2011
258-259 12 p. 687-691
5 p.
article
5 A practical approach to liver metastasis from unknown primary cancer: What surgeons need to know Swaid, Forat
2016
258-259 12 p. 559-566
8 p.
article
6 Asynchronous DNA replication and aneuploidy in lymphocytes of hepatocellular carcinoma patients Hanna, Mariam Onsy F.
2012
258-259 12 p. 636-643
8 p.
article
7 A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma Dadfarnia, Tahereh
2011
258-259 12 p. 666-670
5 p.
article
8 Available technologies and clinical applications of targeted chemotherapy in pancreatic cancer Mukherjee, Indraneil
2016
258-259 12 p. 582-591
10 p.
article
9 Calreticulin mRNA expression and clinicopathological characteristics in acute myeloid leukemia Park, Sholhui
2015
258-259 12 p. 630-635
6 p.
article
10 Clinical application of amplicon-based next-generation sequencing in cancer Chang, Fengqi
2013
258-259 12 p. 413-419
7 p.
article
11 Clinical next generation sequencing in cancer Pfeifer, John D.
2013
258-259 12 p. 409-412
4 p.
article
12 Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemia Zhang, Linsheng
2011
258-259 12 p. 654-665
12 p.
article
13 Cover 1 2013
258-259 12 p. OFC-
1 p.
article
14 Cover 1 2012
258-259 12 p. OFC-
1 p.
article
15 Cover 1 2011
258-259 12 p. OFC-
1 p.
article
16 Cover_spine 2016
258-259 12 p. CO1-
1 p.
article
17 Cover_spine 2015
258-259 12 p. CO1-
1 p.
article
18 Deletion(20q) as the sole abnormality in plasma cell myeloma is not associated with plasma cells as identified by cIg FISH White, Joanne S.
2012
258-259 12 p. 644-652
9 p.
article
19 Design of targeted, capture-based, next generation sequencing tests for precision cancer therapy Hagemann, Ian S.
2013
258-259 12 p. 420-431
12 p.
article
20 Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches Abel, Haley J.
2013
258-259 12 p. 432-440
9 p.
article
21 Duplication of chromosome 1 [dup(1)(q21q32)] as the sole cytogenetic abnormality in a patient previously treated for AML Beach, Douglas F.
2012
258-259 12 p. 665-668
4 p.
article
22 Editorial Board 2013
258-259 12 p. IFC-
1 p.
article
23 Editorial Board 2016
258-259 12 p. CO2-
1 p.
article
24 Editorial Board 2015
258-259 12 p. CO2-
1 p.
article
25 Editorial Board 2012
258-259 12 p. IFC-
1 p.
article
26 Editorial Board 2011
258-259 12 p. IFC-
1 p.
article
27 Effects of PTEN gene alteration in patients with gallbladder cancer Ali, Asgar
2015
258-259 12 p. 587-594
8 p.
article
28 Epidermal growth factor receptor (EGFR) gene copy number in colorectal adenoma-carcinoma progression Flora, Marcella
2012
258-259 12 p. 630-635
6 p.
article
29 Erratum: Long-range massively parallel mate pair sequencing detects distinct mutations and similar patterns of structural mutability in two breast cancer cell lines 2011
258-259 12 p. 694-
1 p.
article
30 Evaluation of the germline single nucleotide polymorphism rs583522 in the TNFAIP3 gene as a prognostic marker in esophageal cancer Ghadban, Tarik
2015
258-259 12 p. 595-601
7 p.
article
31 Genetics of adult glioma Goodenberger, McKinsey L.
2012
258-259 12 p. 613-621
9 p.
article
32 Introduction Kulkarni, Shashikant
2013
258-259 12 p. 407-408
2 p.
article
33 Localization of centromeric breaks in head and neck squamous cell carcinoma Martínez, Jorge García
2012
258-259 12 p. 622-629
8 p.
article
34 Long-term remission of therapy-related acute myeloid leukemia with a new t(11;18)(q23;q21.2) translocation and KMT2A-ME2 (MLL-ME2) fusion gene Szotkowski, Tomáš
2015
258-259 12 p. 610-614
5 p.
article
35 Molecular cytogenetic characterization of epithelioid hemangioendothelioma Woelfel, Cornelius
2011
258-259 12 p. 671-676
6 p.
article
36 Molecular profiles in foregut oncology Sukharamwala, Prashant
2016
258-259 12 p. 537-553
17 p.
article
37 Molecular targeted therapy for pancreatic adenocarcinoma: A review of completed and ongoing late phase clinical trials Mosquera, Catalina
2016
258-259 12 p. 567-581
15 p.
article
38 Mutated MCM9 is associated with predisposition to hereditary mixed polyposis and colorectal cancer in addition to primary ovarian failure Goldberg, Yael
2015
258-259 12 p. 621-624
4 p.
article
39 Sequential transient novel chromosomal translocations in a patient with chronic myelogenous leukemia in complete cytogenetic remission after therapy with imatinib mesylate Papaioannou, George
2011
258-259 12 p. 692-693
2 p.
article
40 Similar cytogenetic findings in two synchronous secondary peripheral chondrosarcomas in a patient with multiple osteochondromas Kyriazoglou, Anastasios I.
2011
258-259 12 p. 677-681
5 p.
article
41 Single nucleotide polymorphism array-based karyotyping shows sequential genomic changes from monosomy to copy-neutral loss of heterozygosity of chromosome 7 and 20q deletion within a balanced translocation t(14;20) in AML Huh, Jungwon
2011
258-259 12 p. 682-686
5 p.
article
42 SNP array and FISH findings in two pleomorphic hyalinizing angiectatic tumors Mohajeri, Arezoo
2012
258-259 12 p. 673-676
4 p.
article
43 Somatic copy number losses on chromosome 9q21.33q22.33 encompassing the PTCH1 loci associated with cardiac fibroma Zhang, Qianqian
2015
258-259 12 p. 615-620
6 p.
article
44 Special issue editorial—Cancer Genetics Rosemurgy, Alexander
2016
258-259 12 p. 535-536
2 p.
article
45 Table of Contents 2013
258-259 12 p. A1-
1 p.
article
46 Table of Contents 2016
258-259 12 p. A1-
1 p.
article
47 Table of Contents 2015
258-259 12 p. A1-
1 p.
article
48 Table of Contents 2012
258-259 12 p. A1-A2
nvt p.
article
49 Table of Contents 2011
258-259 12 p. A1-A2
nvt p.
article
50 The genetics of dyskeratosis congenita Mason, Philip J.
2011
258-259 12 p. 635-645
11 p.
article
51 The pathways of genetic transformation in cholangiocarcinogenesis Serafini, Francesco M.
2016
258-259 12 p. 554-558
5 p.
article
52 The Pro/Pro genotype at TP53 codon 72 polymorphism is associated with early onset glioblastoma El Hallani, Soufiane
2012
258-259 12 p. 677-
1 p.
article
53 Therapy-related pro-B cell acute lymphoblastic leukemia: report of two patients with MLL amplification Racke, Frederick
2012
258-259 12 p. 653-656
4 p.
article
54 Transmission of an expanding donor-derived del(20q) clone through allogeneic hematopoietic stem cell transplantation without the development of a hematologic neoplasm Aikawa, Vania
2015
258-259 12 p. 625-629
5 p.
article
55 Tumor heterogeneity uncovered by dynamic expression of long noncoding RNA at single-cell resolution Hu, Wangxiong
2015
258-259 12 p. 581-586
6 p.
article
56 Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinoma Backsch, Claudia
2011
258-259 12 p. 646-653
8 p.
article
57 Understanding the limitations of next generation sequencing informatics, an approach to clinical pipeline validation using artificial data sets Daber, Robert
2013
258-259 12 p. 441-448
8 p.
article
                             57 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands