| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of gastric adenocarcinoma with conspicuous binuclear cytologic features
|
Ito, Hideaki
|
|
2013
|
216-217 |
7-8 |
p. 304-307
4 p.
|
artikel
|
| 2 |
A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity
|
Jeandidier, Eric
|
|
2012
|
216-217 |
7-8 |
p. 365-372
8 p.
|
artikel
|
| 3 |
Analysis of Esophageal Adenocarcinoma Using Combined aCGH – SNP (CCMC v2+EA) Microarray Platform
|
Ahmad, Ausaf
|
|
2012
|
216-217 |
7-8 |
p. 421-422
2 p.
|
artikel
|
| 4 |
A novel fumarate hydratase-deficient HLRCC kidney cancer cell line, UOK268: a model of the Warburg effect in cancer
|
Yang, Youfeng
|
|
2012
|
216-217 |
7-8 |
p. 377-390
14 p.
|
artikel
|
| 5 |
A polymorphism at the miR-502 binding site in the 3′ untranslated region of the SET8 gene is associated with the risk of epithelial ovarian cancer
|
Wang, Cuiju
|
|
2012
|
216-217 |
7-8 |
p. 373-376
4 p.
|
artikel
|
| 6 |
Array-Based Karyotyping Post Plasma Cell Enrichment for the Detection of Genomic Abnormalities in Multiple Myeloma
|
Zehentner, Barbara K.
|
|
2012
|
216-217 |
7-8 |
p. 419-
1 p.
|
artikel
|
| 7 |
Ascertainment of Recurrent Translocations by Chromosomal Microarray Analysis
|
Gu, Guangyu
|
|
2012
|
216-217 |
7-8 |
p. 420-421
2 p.
|
artikel
|
| 8 |
Atlas of Cytogenomics in Oncology and Hematology: a Platform-Neutral Clinical Cancer Genomics Database
|
Xiang, Bixia
|
|
2012
|
216-217 |
7-8 |
p. 420-
1 p.
|
artikel
|
| 9 |
BCR-PDGFRA fusion in a T lymphoblastic leukemia/lymphoma
|
Yigit, Nuri
|
|
2015
|
216-217 |
7-8 |
p. 404-407
4 p.
|
artikel
|
| 10 |
Change in ploidy status from hyperdiploid to near-tetraploid in multiple myeloma associated with bortezomib/lenalidomide resistance
|
Pavlistova, Lenka
|
|
2014
|
216-217 |
7-8 |
p. 326-331
6 p.
|
artikel
|
| 11 |
Chromosomal aberrations in childhood acute lymphoblastic leukemia: 15-year single center experience
|
Jarosova, Marie
|
|
2016
|
216-217 |
7-8 |
p. 340-347
8 p.
|
artikel
|
| 12 |
Chronic lymphocytic leukemia with a FGFR3 translocation: case report and literature review of an uncommon cytogenetic event
|
Geller, Matthew D.
|
|
2014
|
216-217 |
7-8 |
p. 340-343
4 p.
|
artikel
|
| 13 |
Clinical Laboratory Implementation of the Detection of Genomic Aberrations in Formalin-Fixed Paraffin-Embedded Small Lymphocytic Lymphoma Specimens by Array-CGH
|
Ma, Charles
|
|
2012
|
216-217 |
7-8 |
p. 419-
1 p.
|
artikel
|
| 14 |
Clinical Utility of Single Nucleotide Polymorphism (SNP) Microarrays in Pediatric Cancer and Non-Malignant Hematologic Disorders
|
Lu, Xin-Yan
|
|
2012
|
216-217 |
7-8 |
p. 420-
1 p.
|
artikel
|
| 15 |
Clinicopathology of diffuse intrinsic pontine glioma and its redefined genomic and epigenomic landscape
|
Panditharatna, Eshini
|
|
2015
|
216-217 |
7-8 |
p. 367-373
7 p.
|
artikel
|
| 16 |
Complementation of non-tumorigenicity of HPV18-positive cervical carcinoma cells involves differential mRNA expression of cellular genes including potential tumor suppressor genes on chromosome 11q13
|
Kehrmann, Angela
|
|
2013
|
216-217 |
7-8 |
p. 279-292
14 p.
|
artikel
|
| 17 |
Concordance of copy number alterations using a common analytic pipeline for genome-wide analysis of Illumina and Affymetrix genotyping data: a report from the Children's Oncology Group
|
Vujkovic, Marijana
|
|
2015
|
216-217 |
7-8 |
p. 408-413
6 p.
|
artikel
|
| 18 |
Copy number and expression analysis of FOSL1, GSTP1, NTSR1, FADD and CCND1 genes in primary breast tumors with axillary lymph node metastasis
|
Callegari, Cíntia C.F.
|
|
2016
|
216-217 |
7-8 |
p. 331-339
9 p.
|
artikel
|
| 19 |
Cover 1
|
|
|
2014
|
216-217 |
7-8 |
p. OFC-
1 p.
|
artikel
|
| 20 |
Cover 1
|
|
|
2015
|
216-217 |
7-8 |
p. OFC-
1 p.
|
artikel
|
| 21 |
Cover 1
|
|
|
2013
|
216-217 |
7-8 |
p. OFC-
1 p.
|
artikel
|
| 22 |
Cover 1
|
|
|
2012
|
216-217 |
7-8 |
p. OFC-
1 p.
|
artikel
|
| 23 |
Cover_spine
|
|
|
2016
|
216-217 |
7-8 |
p. CO1-
1 p.
|
artikel
|
| 24 |
Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants
|
Walther, Charles
|
|
2013
|
216-217 |
7-8 |
p. 299-303
5 p.
|
artikel
|
| 25 |
Cytogenetic, fluorescence in situ hybridization, and genomic array characterization of chronic myeloid leukemia with cryptic BCR-ABL1 fusions
|
Shao, Lina
|
|
2015
|
216-217 |
7-8 |
p. 396-403
8 p.
|
artikel
|
| 26 |
Delineating Metastatic Breast Cancer Genome Using Chromosomal Microarray Analysis and Next Generation Sequencing
|
Li, Marilyn M.
|
|
2012
|
216-217 |
7-8 |
p. 422-
1 p.
|
artikel
|
| 27 |
Diagnostic Utility of Array-CGH to Classify Renal Cell Carcinoma in Image-Guided Needle Biopsies
|
Gowrishankar, Banumathy
|
|
2012
|
216-217 |
7-8 |
p. 422-
1 p.
|
artikel
|
| 28 |
Divergent gastrointestinal stromal tumors in syndromic settings
|
Ricci, Riccardo
|
|
2016
|
216-217 |
7-8 |
p. 354-358
5 p.
|
artikel
|
| 29 |
Double minute chromosomes in acute myeloid leukemia, myelodysplastic syndromes, and chronic myelomonocytic leukemia are associated with micronuclei, MYC or MLL amplification, and complex karyotype
|
Huh, Yang O.
|
|
2016
|
216-217 |
7-8 |
p. 313-320
8 p.
|
artikel
|
| 30 |
Editorial Board
|
|
|
2014
|
216-217 |
7-8 |
p. IFC-
1 p.
|
artikel
|
| 31 |
Editorial Board
|
|
|
2015
|
216-217 |
7-8 |
p. A1-
1 p.
|
artikel
|
| 32 |
Editorial Board
|
|
|
2016
|
216-217 |
7-8 |
p. CO2-
1 p.
|
artikel
|
| 33 |
Editorial Board
|
|
|
2013
|
216-217 |
7-8 |
p. IFC-
1 p.
|
artikel
|
| 34 |
Editorial Board
|
|
|
2012
|
216-217 |
7-8 |
p. IFC-
1 p.
|
artikel
|
| 35 |
Evaluation of rs62527607 [GT] single nucleotide polymorphism located in BAALC gene in children with acute leukemia using mismatch PCR-RFLP
|
Nadimi, Motahareh
|
|
2016
|
216-217 |
7-8 |
p. 348-353
6 p.
|
artikel
|
| 36 |
Evaluation of SureFISHtm DNA-FISH Probes for Validation of Array-CGH Aberrations
|
Barenboim, Linda I.
|
|
2012
|
216-217 |
7-8 |
p. 421-
1 p.
|
artikel
|
| 37 |
Ewing sarcoma mimicking atypical carcinoid tumor: detection of unexpected genomic alterations demonstrates the use of next generation sequencing as a diagnostic tool
|
Doyle, Leona A.
|
|
2014
|
216-217 |
7-8 |
p. 335-339
5 p.
|
artikel
|
| 38 |
Exome-level comparison of primary well-differentiated neuroendocrine tumors and their cell lines
|
Boora, Ganesh K.
|
|
2015
|
216-217 |
7-8 |
p. 374-381
8 p.
|
artikel
|
| 39 |
Expression of apoptosis-regulating miRNAs and target mRNAs in oral squamous cell carcinoma
|
Coutinho-Camillo, Cláudia Malheiros
|
|
2015
|
216-217 |
7-8 |
p. 382-389
8 p.
|
artikel
|
| 40 |
Genomic characterization of recurrent high-grade astroblastoma
|
Bale, Tejus A.
|
|
2016
|
216-217 |
7-8 |
p. 321-330
10 p.
|
artikel
|
| 41 |
Genomic Loss of Heterozygosity (LOH) in Pediatric Ovarian Germ Cell Tumors (OGCT)
|
Sutcliffe, Maxine J.
|
|
2012
|
216-217 |
7-8 |
p. 423-424
2 p.
|
artikel
|
| 42 |
Genomic microarray analysis on formalin-fixed paraffin-embedded material for uveal melanoma prognostication
|
Minca, Eugen C.
|
|
2014
|
216-217 |
7-8 |
p. 306-315
10 p.
|
artikel
|
| 43 |
HELIOS-BCL11B fusion gene involvement in a t(2;14)(q34;q32) in an adult T-cell leukemia patient
|
Fujimoto, Rika
|
|
2012
|
216-217 |
7-8 |
p. 356-364
9 p.
|
artikel
|
| 44 |
Hyperhaploid plasma cell myeloma
|
Hoctor, Veronica T.
|
|
2012
|
216-217 |
7-8 |
p. 414-418
5 p.
|
artikel
|
| 45 |
IGF2BP1: a novel IGH translocation partner in B acute lymphoblastic leukemia
|
Gu, Guangyu
|
|
2014
|
216-217 |
7-8 |
p. 332-334
3 p.
|
artikel
|
| 46 |
Low incidence of IL6ST (gp130) mutations in exon 6 in lung cancer of a Chinese cohort
|
Sun, Luguo
|
|
2014
|
216-217 |
7-8 |
p. 291-298
8 p.
|
artikel
|
| 47 |
Methylenetetrahydrofolate reductase gene polymorphisms and skin cancer risk: a meta-analysis
|
Deng, Feng
|
|
2014
|
216-217 |
7-8 |
p. 299-305
7 p.
|
artikel
|
| 48 |
Molecular analysis distinguishes metastatic disease from second cancers in patients with retinoblastoma
|
Racher, Hilary
|
|
2016
|
216-217 |
7-8 |
p. 359-363
5 p.
|
artikel
|
| 49 |
Molecular classification, pathway addiction, and therapeutic targeting in diffuse large B cell lymphoma
|
Puvvada, Soham
|
|
2013
|
216-217 |
7-8 |
p. 257-265
9 p.
|
artikel
|
| 50 |
Molecular genetic characterization of the 11q13 breakpoint in a desmoplastic fibroma of bone
|
Trombetta, Domenico
|
|
2012
|
216-217 |
7-8 |
p. 410-413
4 p.
|
artikel
|
| 51 |
Molecular inversion probe analysis detects novel copy number alterations in Ewing sarcoma
|
Jahromi, Mona S.
|
|
2012
|
216-217 |
7-8 |
p. 391-404
14 p.
|
artikel
|
| 52 |
Molecular inversion probes: a novel microarray technology and its application in cancer research
|
Wang, Yuker
|
|
2012
|
216-217 |
7-8 |
p. 341-355
15 p.
|
artikel
|
| 53 |
Narrowing down the common deleted region of 5q to 6.0 Mb in blastic plasmacytoid dendritic cell neoplasms
|
Fu, Yumei
|
|
2013
|
216-217 |
7-8 |
p. 293-298
6 p.
|
artikel
|
| 54 |
Polymorphisms in genes related to inflammation, NSAID use, and the risk of prostate cancer among Danish men
|
Kopp, Tine Iskov
|
|
2013
|
216-217 |
7-8 |
p. 266-278
13 p.
|
artikel
|
| 55 |
Population-based characterization of the genetic landscape of chronic lymphocytic leukemia patients referred for cytogenetic testing in British Columbia, Canada: the role of provincial laboratory standardization
|
Gerrie, Alina S.
|
|
2014
|
216-217 |
7-8 |
p. 316-325
10 p.
|
artikel
|
| 56 |
Recurrent Genetic Alterations in Hepatitis C-associated Hepatocellular Carcinoma Detected by CGH+SNP Array
|
Liu, Yajuan
|
|
2012
|
216-217 |
7-8 |
p. 423-
1 p.
|
artikel
|
| 57 |
SNP Array Analysis Detects Genomic Alterations Associated with High-Risk Disease in Neuroblastoma
|
Ouyang, Karen J.
|
|
2012
|
216-217 |
7-8 |
p. 423-
1 p.
|
artikel
|
| 58 |
Somatic c.34G>T KRAS mutation: a new prescreening test for MUTYH-associated polyposis?
|
Aimé, Adeline
|
|
2015
|
216-217 |
7-8 |
p. 390-395
6 p.
|
artikel
|
| 59 |
Table of Contents
|
|
|
2014
|
216-217 |
7-8 |
p. A1-
1 p.
|
artikel
|
| 60 |
Table of Contents
|
|
|
2015
|
216-217 |
7-8 |
p. A3-
1 p.
|
artikel
|
| 61 |
Table of Contents
|
|
|
2016
|
216-217 |
7-8 |
p. A1-
1 p.
|
artikel
|
| 62 |
Table of Contents
|
|
|
2013
|
216-217 |
7-8 |
p. A1-
1 p.
|
artikel
|
| 63 |
Table of Contents
|
|
|
2012
|
216-217 |
7-8 |
p. A1-A2
nvt p.
|
artikel
|
| 64 |
The HEL Erythroleukemia Cell Line as a Test Case for Detailed Description of a Complex Karyotype by Combining SNP Array with Multiple FISH Approaches
|
MacKinnon, Ruth N.
|
|
2012
|
216-217 |
7-8 |
p. 421-
1 p.
|
artikel
|
| 65 |
The NAB2–STAT6 gene fusion in solitary fibrous tumor can be reliably detected by anchored multiplexed PCR for targeted next-generation sequencing
|
Guseva, Natalya V.
|
|
2016
|
216-217 |
7-8 |
p. 303-312
10 p.
|
artikel
|
| 66 |
Validation of Karyotypic Abnormalities in Human Pluripotent Stem Cells: Cytogenetic Progression in WA09 Mirrors Cancer
|
Nisler, Benjamin S.
|
|
2012
|
216-217 |
7-8 |
p. 423-
1 p.
|
artikel
|
| 67 |
When are apparently non-clonal abnormalities in bone marrow chromosome studies actually clonal?
|
Hutchens, Chandra
|
|
2012
|
216-217 |
7-8 |
p. 405-409
5 p.
|
artikel
|
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