Digitale Bibliotheek
Sluiten Bladeren door artikelen uit een tijdschrift
     Tijdschrift beschrijving
       Alle jaargangen van het bijbehorende tijdschrift
         Alle afleveringen van het bijbehorende jaargang
                                       Alle artikelen van de bijbehorende aflevering
 
                             57 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Aberrant methylation of the TERT promoter in esophageal squamous cell carcinoma Deng, Jiaying
2015
216-217 12 p. 602-609
8 p.
artikel
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
216-217 12 p. 657-664
8 p.
artikel
3 A novel TCF3-HLF fusion transcript in acute lymphoblastic leukemia with a t(17;19)(q22;p13) Panagopoulos, Ioannis
2012
216-217 12 p. 669-672
4 p.
artikel
4 A possible 5′-NRIP1/UHRF1-3′ fusion gene detected by array CGH analysis in a Ph+ ALL patient Zhang, Rui
2011
216-217 12 p. 687-691
5 p.
artikel
5 A practical approach to liver metastasis from unknown primary cancer: What surgeons need to know Swaid, Forat
2016
216-217 12 p. 559-566
8 p.
artikel
6 Asynchronous DNA replication and aneuploidy in lymphocytes of hepatocellular carcinoma patients Hanna, Mariam Onsy F.
2012
216-217 12 p. 636-643
8 p.
artikel
7 A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma Dadfarnia, Tahereh
2011
216-217 12 p. 666-670
5 p.
artikel
8 Available technologies and clinical applications of targeted chemotherapy in pancreatic cancer Mukherjee, Indraneil
2016
216-217 12 p. 582-591
10 p.
artikel
9 Calreticulin mRNA expression and clinicopathological characteristics in acute myeloid leukemia Park, Sholhui
2015
216-217 12 p. 630-635
6 p.
artikel
10 Clinical application of amplicon-based next-generation sequencing in cancer Chang, Fengqi
2013
216-217 12 p. 413-419
7 p.
artikel
11 Clinical next generation sequencing in cancer Pfeifer, John D.
2013
216-217 12 p. 409-412
4 p.
artikel
12 Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemia Zhang, Linsheng
2011
216-217 12 p. 654-665
12 p.
artikel
13 Cover 1 2013
216-217 12 p. OFC-
1 p.
artikel
14 Cover 1 2012
216-217 12 p. OFC-
1 p.
artikel
15 Cover 1 2011
216-217 12 p. OFC-
1 p.
artikel
16 Cover_spine 2016
216-217 12 p. CO1-
1 p.
artikel
17 Cover_spine 2015
216-217 12 p. CO1-
1 p.
artikel
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
216-217 12 p. 644-652
9 p.
artikel
19 Design of targeted, capture-based, next generation sequencing tests for precision cancer therapy Hagemann, Ian S.
2013
216-217 12 p. 420-431
12 p.
artikel
20 Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches Abel, Haley J.
2013
216-217 12 p. 432-440
9 p.
artikel
21 Duplication of chromosome 1 [dup(1)(q21q32)] as the sole cytogenetic abnormality in a patient previously treated for AML Beach, Douglas F.
2012
216-217 12 p. 665-668
4 p.
artikel
22 Editorial Board 2013
216-217 12 p. IFC-
1 p.
artikel
23 Editorial Board 2016
216-217 12 p. CO2-
1 p.
artikel
24 Editorial Board 2015
216-217 12 p. CO2-
1 p.
artikel
25 Editorial Board 2012
216-217 12 p. IFC-
1 p.
artikel
26 Editorial Board 2011
216-217 12 p. IFC-
1 p.
artikel
27 Effects of PTEN gene alteration in patients with gallbladder cancer Ali, Asgar
2015
216-217 12 p. 587-594
8 p.
artikel
28 Epidermal growth factor receptor (EGFR) gene copy number in colorectal adenoma-carcinoma progression Flora, Marcella
2012
216-217 12 p. 630-635
6 p.
artikel
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
216-217 12 p. 694-
1 p.
artikel
30 Evaluation of the germline single nucleotide polymorphism rs583522 in the TNFAIP3 gene as a prognostic marker in esophageal cancer Ghadban, Tarik
2015
216-217 12 p. 595-601
7 p.
artikel
31 Genetics of adult glioma Goodenberger, McKinsey L.
2012
216-217 12 p. 613-621
9 p.
artikel
32 Introduction Kulkarni, Shashikant
2013
216-217 12 p. 407-408
2 p.
artikel
33 Localization of centromeric breaks in head and neck squamous cell carcinoma Martínez, Jorge García
2012
216-217 12 p. 622-629
8 p.
artikel
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
216-217 12 p. 610-614
5 p.
artikel
35 Molecular cytogenetic characterization of epithelioid hemangioendothelioma Woelfel, Cornelius
2011
216-217 12 p. 671-676
6 p.
artikel
36 Molecular profiles in foregut oncology Sukharamwala, Prashant
2016
216-217 12 p. 537-553
17 p.
artikel
37 Molecular targeted therapy for pancreatic adenocarcinoma: A review of completed and ongoing late phase clinical trials Mosquera, Catalina
2016
216-217 12 p. 567-581
15 p.
artikel
38 Mutated MCM9 is associated with predisposition to hereditary mixed polyposis and colorectal cancer in addition to primary ovarian failure Goldberg, Yael
2015
216-217 12 p. 621-624
4 p.
artikel
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
216-217 12 p. 692-693
2 p.
artikel
40 Similar cytogenetic findings in two synchronous secondary peripheral chondrosarcomas in a patient with multiple osteochondromas Kyriazoglou, Anastasios I.
2011
216-217 12 p. 677-681
5 p.
artikel
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
216-217 12 p. 682-686
5 p.
artikel
42 SNP array and FISH findings in two pleomorphic hyalinizing angiectatic tumors Mohajeri, Arezoo
2012
216-217 12 p. 673-676
4 p.
artikel
43 Somatic copy number losses on chromosome 9q21.33q22.33 encompassing the PTCH1 loci associated with cardiac fibroma Zhang, Qianqian
2015
216-217 12 p. 615-620
6 p.
artikel
44 Special issue editorial—Cancer Genetics Rosemurgy, Alexander
2016
216-217 12 p. 535-536
2 p.
artikel
45 Table of Contents 2013
216-217 12 p. A1-
1 p.
artikel
46 Table of Contents 2016
216-217 12 p. A1-
1 p.
artikel
47 Table of Contents 2015
216-217 12 p. A1-
1 p.
artikel
48 Table of Contents 2012
216-217 12 p. A1-A2
nvt p.
artikel
49 Table of Contents 2011
216-217 12 p. A1-A2
nvt p.
artikel
50 The genetics of dyskeratosis congenita Mason, Philip J.
2011
216-217 12 p. 635-645
11 p.
artikel
51 The pathways of genetic transformation in cholangiocarcinogenesis Serafini, Francesco M.
2016
216-217 12 p. 554-558
5 p.
artikel
52 The Pro/Pro genotype at TP53 codon 72 polymorphism is associated with early onset glioblastoma El Hallani, Soufiane
2012
216-217 12 p. 677-
1 p.
artikel
53 Therapy-related pro-B cell acute lymphoblastic leukemia: report of two patients with MLL amplification Racke, Frederick
2012
216-217 12 p. 653-656
4 p.
artikel
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
216-217 12 p. 625-629
5 p.
artikel
55 Tumor heterogeneity uncovered by dynamic expression of long noncoding RNA at single-cell resolution Hu, Wangxiong
2015
216-217 12 p. 581-586
6 p.
artikel
56 Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinoma Backsch, Claudia
2011
216-217 12 p. 646-653
8 p.
artikel
57 Understanding the limitations of next generation sequencing informatics, an approach to clinical pipeline validation using artificial data sets Daber, Robert
2013
216-217 12 p. 441-448
8 p.
artikel
                             57 gevonden resultaten
 
 Koninklijke Bibliotheek - Nationale Bibliotheek van Nederland