| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Advances in the understanding of constitutional and somatic genomic alterations in neuroblastoma
|
Deyell, Rebecca J.
|
|
2011
|
216-217 |
3 |
p. 113-121
9 p.
|
artikel
|
| 2 |
Amplification of EVI1 on cytogenetically cryptic double minutes as new mechanism for increased expression of EVI1
|
Volkert, Sarah
|
|
2014
|
216-217 |
3 |
p. 103-108
6 p.
|
artikel
|
| 3 |
Analysis of miRNA-gene expression-genomic profiles reveals complex mechanisms of microRNA deregulation in osteosarcoma
|
Maire, Georges
|
|
2011
|
216-217 |
3 |
p. 138-146
9 p.
|
artikel
|
| 4 |
A new rearrangement giving rise to a very rare MLL-MLLT10 fusion mRNA in an infant acute myeloid leukemia
|
Burillo-Sanz, Sergio
|
|
2015
|
216-217 |
3 |
p. 101-102
2 p.
|
artikel
|
| 5 |
A novel BAP1 mutation is associated with melanocytic neoplasms and thyroid cancer
|
McDonnell, Kevin J.
|
|
2016
|
216-217 |
3 |
p. 75-81
7 p.
|
artikel
|
| 6 |
A t(11;14)(p13;q11.2) in myelofibrosis following polycythemia vera
|
Jeong, Ji Hun
|
|
2016
|
216-217 |
3 |
p. 112-116
5 p.
|
artikel
|
| 7 |
BCL2, BCL6, IGH, TP53, and MYC protein expression and gene rearrangements as prognostic markers in diffuse large B-cell lymphoma: a study of 44 Turkish patients
|
Akay, Olga Meltem
|
|
2014
|
216-217 |
3 |
p. 87-93
7 p.
|
artikel
|
| 8 |
CD5-positive, cyclinD1-negative mantle cell lymphoma with a translocation involving the CCND2 gene and the IGL locus
|
Shiller, Shirley Michelle
|
|
2011
|
216-217 |
3 |
p. 162-164
3 p.
|
artikel
|
| 9 |
Chronic lymphocytic leukemia: a clinical and molecular heterogenous disease
|
Rodríguez-Vicente, Ana E.
|
|
2013
|
216-217 |
3 |
p. 49-62
14 p.
|
artikel
|
| 10 |
Clinical significance of papillary thyroid cancer risk loci identified by genome-wide association studies
|
Wei, Wen-Jun
|
|
2015
|
216-217 |
3 |
p. 68-75
8 p.
|
artikel
|
| 11 |
Clonal chromosomal abnormalities in Ph-negative cells in chronic myeloid leukemia: an unusual case evolving to secondary acute myeloid leukemia
|
Van Obbergh, Florence
|
|
2015
|
216-217 |
3 |
p. 102-104
3 p.
|
artikel
|
| 12 |
Combinations of genetic data in a study of neuroblastoma risk genotypes
|
Capasso, Mario
|
|
2014
|
216-217 |
3 |
p. 94-97
4 p.
|
artikel
|
| 13 |
Comparison of chromosomal aberrations in primary colorectal carcinomas to their pulmonary metastases
|
Danner, Bernhard C.
|
|
2011
|
216-217 |
3 |
p. 122-128
7 p.
|
artikel
|
| 14 |
Constance A. Griffin, MD (June 8, 1951–January 8, 2012)
|
Axilbund, Jennifer E.
|
|
2012
|
216-217 |
3 |
p. 78-79
2 p.
|
artikel
|
| 15 |
Copy neutral loss of heterozygosity in 20q in chronic lymphocytic leukemia/small lymphocytic lymphoma
|
Pei, Jianming
|
|
2014
|
216-217 |
3 |
p. 98-102
5 p.
|
artikel
|
| 16 |
Cover 1
|
|
|
2015
|
216-217 |
3 |
p. OFC-
1 p.
|
artikel
|
| 17 |
Cover 1
|
|
|
2012
|
216-217 |
3 |
p. OFC-
1 p.
|
artikel
|
| 18 |
Cover 1
|
|
|
2011
|
216-217 |
3 |
p. OFC-
1 p.
|
artikel
|
| 19 |
Cover 1
|
|
|
2013
|
216-217 |
3 |
p. OFC-
1 p.
|
artikel
|
| 20 |
Cover 1
|
|
|
2014
|
216-217 |
3 |
p. OFC-
1 p.
|
artikel
|
| 21 |
Cover_spine
|
|
|
2016
|
216-217 |
3 |
p. CO1-
1 p.
|
artikel
|
| 22 |
Crizotinib resistance in acute myeloid leukemia with inv(2)(p23q13)/RAN binding protein 2 (RANBP2) anaplastic lymphoma kinase (ALK) fusion and monosomy 7
|
Takeoka, Kayo
|
|
2015
|
216-217 |
3 |
p. 85-90
6 p.
|
artikel
|
| 23 |
Cytogenetic abnormalities and monosomal karyotypes in children and adolescents with acute myeloid leukemia: correlations with clinical characteristics and outcome
|
Manola, Kalliopi N.
|
|
2013
|
216-217 |
3 |
p. 63-72
10 p.
|
artikel
|
| 24 |
Development of t(8;21) and RUNX1–RUNX1T1 in the Philadelphia-positive clone of a patient with chronic myelogenous leukemia: additional evidence for multiple steps involved in disease progression
|
Najfeld, Vesna
|
|
2011
|
216-217 |
3 |
p. 165-170
6 p.
|
artikel
|
| 25 |
Disruption of the APC gene by t(5;7) translocation in a Turcot family
|
Sahnane, Nora
|
|
2016
|
216-217 |
3 |
p. 107-111
5 p.
|
artikel
|
| 26 |
Distinct set of chromosomal aberrations in childhood hepatocellular carcinoma is correlated to hepatitis B virus infection
|
Tan, Lu
|
|
2016
|
216-217 |
3 |
p. 87-96
10 p.
|
artikel
|
| 27 |
Down-regulation of FoxM1 leads to the inhibition of the epithelial-mesenchymal transition in gastric cancer cells
|
Miao, Lifeng
|
|
2014
|
216-217 |
3 |
p. 75-82
8 p.
|
artikel
|
| 28 |
Editorial Board
|
|
|
2014
|
216-217 |
3 |
p. IFC-
1 p.
|
artikel
|
| 29 |
Editorial Board
|
|
|
2015
|
216-217 |
3 |
p. IFC-
1 p.
|
artikel
|
| 30 |
Editorial Board
|
|
|
2016
|
216-217 |
3 |
p. CO2-
1 p.
|
artikel
|
| 31 |
Editorial Board
|
|
|
2012
|
216-217 |
3 |
p. A1-
1 p.
|
artikel
|
| 32 |
Editorial Board
|
|
|
2011
|
216-217 |
3 |
p. IFC-
1 p.
|
artikel
|
| 33 |
Editorial Board
|
|
|
2013
|
216-217 |
3 |
p. IFC-
1 p.
|
artikel
|
| 34 |
Effectiveness of dasatinib in accelerated-phase chronic myeloid leukemia with p190 BCR-ABL1 and a second Philadelphia chromosome
|
Rabenau, Karen E.
|
|
2014
|
216-217 |
3 |
p. 109-110
2 p.
|
artikel
|
| 35 |
Evolution in a transmissible cancer: a study of the chromosomal changes in devil facial tumor (DFT) as it spreads through the wild Tasmanian devil population
|
Pearse, Anne-Maree
|
|
2012
|
216-217 |
3 |
p. 101-112
12 p.
|
artikel
|
| 36 |
Expression of Kit and Etv1 in restricted brain regions supports a brain-cell progenitor as an origin for cranial germinomas
|
Tan, Chris
|
|
2015
|
216-217 |
3 |
p. 55-61
7 p.
|
artikel
|
| 37 |
High frequency of allelic loss at the BRCA1 locus in ovarian cancers: clinicopathologic and molecular associations
|
Rzepecka, Iwona K.
|
|
2012
|
216-217 |
3 |
p. 94-100
7 p.
|
artikel
|
| 38 |
High resolution array comparative genomic hybridization identifies copy number alterations in diffuse large B-cell lymphoma that predict response to immuno-chemotherapy
|
Kreisel, F.
|
|
2011
|
216-217 |
3 |
p. 129-137
9 p.
|
artikel
|
| 39 |
Identification of the TAF15–ZNF384 fusion gene in two new cases of acute lymphoblastic leukemia with a t(12;17)(p13;q12)
|
Nyquist, Kaja Beate
|
|
2011
|
216-217 |
3 |
p. 147-152
6 p.
|
artikel
|
| 40 |
Investigation of a putative melanoma susceptibility locus at chromosome 3q29
|
Tuominen, Rainer
|
|
2014
|
216-217 |
3 |
p. 70-74
5 p.
|
artikel
|
| 41 |
Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia
|
Gorello, Paolo
|
|
2013
|
216-217 |
3 |
p. 92-96
5 p.
|
artikel
|
| 42 |
Matrix metalloproteinase 13: a potential intermediate between low expression of microRNA-125b and increasing metastatic potential of non–small cell lung cancer
|
Yu, Xiaozhou
|
|
2015
|
216-217 |
3 |
p. 76-84
9 p.
|
artikel
|
| 43 |
Melanoma risk associated with MC1R gene variants in Latvia and the functional analysis of rare variants
|
Ozola, Aija
|
|
2013
|
216-217 |
3 |
p. 81-91
11 p.
|
artikel
|
| 44 |
MicroRNA-26a regulates tumorigenic properties of EZH2 in human lung carcinoma cells
|
Dang, Xiaomin
|
|
2012
|
216-217 |
3 |
p. 113-123
11 p.
|
artikel
|
| 45 |
Monosomy and ring chromosome 13 in a thyroid nodular goiter—do we underestimate its relevance in benign thyroid lesions?
|
Sendt, Wolfgang
|
|
2012
|
216-217 |
3 |
p. 128-130
3 p.
|
artikel
|
| 46 |
MYC amplification in multiple marker chromosomes and EZH2 microdeletion in a man with acute myeloid leukemia
|
Xiang, Zhifu
|
|
2015
|
216-217 |
3 |
p. 96-100
5 p.
|
artikel
|
| 47 |
Oncogenic KIAA1549-BRAF fusion with activation of the MAPK/ERK pathway in pediatric oligodendrogliomas
|
Kumar, Anupam
|
|
2015
|
216-217 |
3 |
p. 91-95
5 p.
|
artikel
|
| 48 |
Optimal strategy for obtaining routine chromosome analysis by using negative fractions of CD138 enriched plasma cells
|
Ortega, Veronica
|
|
2016
|
216-217 |
3 |
p. 82-86
5 p.
|
artikel
|
| 49 |
Overview of recurrent chromosomal losses in retinoblastoma detected by low coverage next generation sequencing
|
García-Chequer, A.J.
|
|
2016
|
216-217 |
3 |
p. 57-69
13 p.
|
artikel
|
| 50 |
22q11-q13 as a hot spot for prediction of disease-free survival in bile duct cancer: integrative analysis of copy number variations
|
Kang, Mee Joo
|
|
2014
|
216-217 |
3 |
p. 57-69
13 p.
|
artikel
|
| 51 |
Rare germline variant (rs78378222) in the TP53 3' UTR: Evidence for a new mechanism of cancer predisposition in Li-Fraumeni syndrome
|
Macedo, Gabriel S.
|
|
2016
|
216-217 |
3 |
p. 97-106
10 p.
|
artikel
|
| 52 |
Simultaneous occurrence of ETV6-RUNX1 and BCR-ABL1 (e1a2) transcripts in a child with B-cell acute lymphoblastic leukemia
|
Balatzenko, Gueorgui
|
|
2013
|
216-217 |
3 |
p. 97-101
5 p.
|
artikel
|
| 53 |
SNP-based arrays complement classic cytogenetics in the detection of chromosomal aberrations in Wilms’ tumor
|
Zin, Reena
|
|
2012
|
216-217 |
3 |
p. 80-93
14 p.
|
artikel
|
| 54 |
Somatic loss of an EXT2 gene mutation during malignant progression in a patient with hereditary multiple osteochondromas
|
Musso, Nicolò
|
|
2015
|
216-217 |
3 |
p. 62-67
6 p.
|
artikel
|
| 55 |
Table of Contents
|
|
|
2014
|
216-217 |
3 |
p. A1-
1 p.
|
artikel
|
| 56 |
Table of Contents
|
|
|
2015
|
216-217 |
3 |
p. A1-
1 p.
|
artikel
|
| 57 |
Table of Contents
|
|
|
2016
|
216-217 |
3 |
p. A1-
1 p.
|
artikel
|
| 58 |
Table of Contents
|
|
|
2012
|
216-217 |
3 |
p. A3-
1 p.
|
artikel
|
| 59 |
Table of Contents
|
|
|
2011
|
216-217 |
3 |
p. A1-A2
nvt p.
|
artikel
|
| 60 |
Table of Contents
|
|
|
2013
|
216-217 |
3 |
p. A1-
1 p.
|
artikel
|
| 61 |
The characteristics and prognostic analysis in 213 myeloid malignancy patients with del(20q): a report of a single-center case series
|
Pan, Jinlan
|
|
2014
|
216-217 |
3 |
p. 51-56
6 p.
|
artikel
|
| 62 |
The first case of Philadelphia chromosome-negative acute promyelocytic leukemia following imatinib for chronic myelogenous leukemia
|
Wakim, Jad J.
|
|
2012
|
216-217 |
3 |
p. 124-127
4 p.
|
artikel
|
| 63 |
The genetics of gestational trophoblastic disease: a rare complication of pregnancy
|
Hoffner, Lori
|
|
2012
|
216-217 |
3 |
p. 63-77
15 p.
|
artikel
|
| 64 |
The peculiar 11q-gain/loss aberration reported in a subset of MYC-negative high-grade B-cell lymphomas can also occur in a MYC-rearranged lymphoma
|
Havelange, Violaine
|
|
2016
|
216-217 |
3 |
p. 117-118
2 p.
|
artikel
|
| 65 |
The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers
|
Laitman, Yael
|
|
2016
|
216-217 |
3 |
p. 70-74
5 p.
|
artikel
|
| 66 |
Translocation t(2;7)(p11;q21) associated with the CDK6/IGK rearrangement is a rare but recurrent abnormality in B-cell lymphoproliferative malignancies
|
Douet-Guilbert, Nathalie
|
|
2014
|
216-217 |
3 |
p. 83-86
4 p.
|
artikel
|
| 67 |
Unbalanced translocations of 20q in AML and MDS often involve interstitial rather than terminal deletions of 20q
|
MacKinnon, Ruth N.
|
|
2011
|
216-217 |
3 |
p. 153-161
9 p.
|
artikel
|
| 68 |
Utility of serum DNA and pyrosequencing for the detection of EGFR mutations in non-small cell lung cancer
|
Akca, Hakan
|
|
2013
|
216-217 |
3 |
p. 73-80
8 p.
|
artikel
|
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