nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A complex MLL rearrangement identified five years after initial MDS diagnosis results in out-of-frame fusions without progression to acute leukemia
|
Meyer, Claus |
|
2011 |
|
10 |
p. 557-562 6 p. |
artikel |
2 |
Acquired genomic copy number changes in CML patients with the Philadelphia chromosome (Ph+)
|
Lu, Xianglan |
|
2012 |
|
10 |
p. 513-518 6 p. |
artikel |
3 |
An asbestos-exposed family with multiple cases of pleural malignant mesothelioma without inheritance of a predisposing BAP1 mutation
|
Cheung, Mitchell |
|
2015 |
|
10 |
p. 502-507 6 p. |
artikel |
4 |
A new NFIA:RAF1 fusion activating the MAPK pathway in pilocytic astrocytoma
|
Yde, Christina Westmose |
|
2016 |
|
10 |
p. 440-444 5 p. |
artikel |
5 |
An optimized technology platform for the rapid multiplex molecular analysis of genetic alterations associated with leukemia
|
Ye, Fei |
|
2012 |
|
10 |
p. 488-500 13 p. |
artikel |
6 |
A novel FOXP1-PDGFRA fusion gene in myeloproliferative neoplasm with eosinophilia
|
Sugimoto, Yuka |
|
2015 |
|
10 |
p. 508-512 5 p. |
artikel |
7 |
A simple bone cyst of the distal humerus with a t(7;12)(q21;q24.3) in a patient with hypophosphatemic rickets
|
Sakai Junior, Nilo |
|
2012 |
|
10 |
p. 541-543 3 p. |
artikel |
8 |
Association of polymorphisms in microRNA-binding sites and colorectal cancer in an Iranian population
|
Azimzadeh, Pedram |
|
2012 |
|
10 |
p. 501-507 7 p. |
artikel |
9 |
Case of polycythemia vera concurrent with FIP1L1-PDGFRA–positive myeloproliferative neoplasm with eosinophilia
|
Alrwas, Anas |
|
2012 |
|
10 |
p. 519-522 4 p. |
artikel |
10 |
Caspase 9 promoter polymorphisms confer increased susceptibility to breast cancer
|
Theodoropoulos, George E. |
|
2012 |
|
10 |
p. 508-512 5 p. |
artikel |
11 |
Chronic myelogenous leukemia with acquired t(11;14)(q13;q32) CCND1-IGH: A case report and literature review
|
Manda-Mapalo, M.T. |
|
2016 |
|
10 |
p. 481-485 5 p. |
artikel |
12 |
Clinical and molecular cytogenetic studies in ten patients with hematological malignancies characterized by t(20;21)(q11;q11) resulted from del(20q)
|
Wu, Chunxiao |
|
2016 |
|
10 |
p. 456-462 7 p. |
artikel |
13 |
Co-localized genomic regulation of miRNA and mRNA via DNA methylation affects survival in multiple tumor types
|
Doecke, James D. |
|
2016 |
|
10 |
p. 463-473 11 p. |
artikel |
14 |
Comparative transcriptome analysis reveals that the extracellular matrix receptor interaction contributes to the venous metastases of hepatocellular carcinoma
|
Zhang, Hong |
|
2015 |
|
10 |
p. 482-491 10 p. |
artikel |
15 |
Cover 1
|
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|
2012 |
|
10 |
p. OFC- 1 p. |
artikel |
16 |
Cover 1
|
|
|
2011 |
|
10 |
p. OFC- 1 p. |
artikel |
17 |
Cover_spine
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|
2015 |
|
10 |
p. CO1- 1 p. |
artikel |
18 |
Cover_spine
|
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|
2016 |
|
10 |
p. CO1- 1 p. |
artikel |
19 |
Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia
|
Pierini, Valentina |
|
2011 |
|
10 |
p. 563-568 6 p. |
artikel |
20 |
Editorial Board
|
|
|
2012 |
|
10 |
p. IFC- 1 p. |
artikel |
21 |
Editorial Board
|
|
|
2015 |
|
10 |
p. CO2- 1 p. |
artikel |
22 |
Editorial Board
|
|
|
2016 |
|
10 |
p. CO2- 1 p. |
artikel |
23 |
Editorial Board
|
|
|
2011 |
|
10 |
p. IFC- 1 p. |
artikel |
24 |
Evaluation of CTNNB1 and TP53 variability in patients with hepatocellular carcinoma and occult hepatitis B virus infection
|
Saitta, Carlo |
|
2015 |
|
10 |
p. 513-516 4 p. |
artikel |
25 |
Frequency of copy number abnormalities in common genes associated with B-cell precursor acute lymphoblastic leukemia cytogenetic subtypes in Brazilian children
|
Conceição Barbosa, Thayana |
|
2015 |
|
10 |
p. 492-501 10 p. |
artikel |
26 |
Genotyping and differential expression analysis of inflammasome genes in sporadic malignant melanoma reveal novel contribution of CARD8, IL1B and IL18 in melanoma susceptibility and progression
|
da Silva, Wanessa Cardoso |
|
2016 |
|
10 |
p. 474-480 7 p. |
artikel |
27 |
High resolution genomic profiling and classical cytogenetics in a group of benign and atypical meningiomas
|
Holland, Heidrun |
|
2011 |
|
10 |
p. 541-549 9 p. |
artikel |
28 |
HMGA2 and MDM2 expression in lipomatous tumors with partial, low-level amplification of sequences from the long arm of chromosome 12
|
Mandahl, Nils |
|
2011 |
|
10 |
p. 550-556 7 p. |
artikel |
29 |
Immunoglobulin heavy chain (IGH@) translocations negatively impact treatment-free survival for chronic lymphocytic leukemia patients who have an isolated deletion 13q abnormality
|
Gerrie, Alina S. |
|
2012 |
|
10 |
p. 523-527 5 p. |
artikel |
30 |
Integrative genomic analysis identifies CCNB1 and CDC2 as candidate genes associated with meningioma recurrence
|
Bie, Li |
|
2011 |
|
10 |
p. 536-540 5 p. |
artikel |
31 |
Li-Fraumeni syndrome: report of a clinical research workshop and creation of a research consortium
|
Mai, Phuong L. |
|
2012 |
|
10 |
p. 479-487 9 p. |
artikel |
32 |
Microarray, gene sequencing, and reverse transcriptase–polymerase chain reaction analyses of a cryptic PML-RARA translocation
|
Koshy, Jason |
|
2012 |
|
10 |
p. 537-540 4 p. |
artikel |
33 |
Molecular cytogenetics of pediatric adipocytic tumors
|
Dadone, Bérengère |
|
2015 |
|
10 |
p. 469-481 13 p. |
artikel |
34 |
MYC rearranged B-cell neoplasms: Impact of genetics on classification
|
Haberl, Sabine |
|
2016 |
|
10 |
p. 431-439 9 p. |
artikel |
35 |
Myelodysplastic syndrome with a t(2;11)(p21;q23-24) and translocation breakpoint close to miR-125b-1
|
Thorsen, Jim |
|
2012 |
|
10 |
p. 528-532 5 p. |
artikel |
36 |
Next generation exome sequencing of pancreatic neuroendocrine tumor cell lines BON-1 and QGP-1 reveals different lineages
|
Vandamme, Timon |
|
2015 |
|
10 |
p. 523- 1 p. |
artikel |
37 |
Overexpression of the LSAMP and TUSC7 genes in acute myeloid leukemia following microdeletion/duplication of chromosome 3
|
Coccaro, Nicoletta |
|
2015 |
|
10 |
p. 517-522 6 p. |
artikel |
38 |
Secondary acute myelogenous leukemia (AML) with trisomy 10 and del(9q) following precursor B-cell acute lymphoblastic leukemia (ALL) with a hyperdiploid karyotype
|
Al-Tahou, Karima |
|
2012 |
|
10 |
p. 533-536 4 p. |
artikel |
39 |
Table of Contents
|
|
|
2012 |
|
10 |
p. A1-A2 nvt p. |
artikel |
40 |
Table of Contents
|
|
|
2015 |
|
10 |
p. A1- 1 p. |
artikel |
41 |
Table of Contents
|
|
|
2016 |
|
10 |
p. A1- 1 p. |
artikel |
42 |
Table of Contents
|
|
|
2011 |
|
10 |
p. A1- 1 p. |
artikel |
43 |
Targeting genetic and epigenetic alterations in the treatment of serous ovarian cancer
|
Weberpals, Johanne I. |
|
2011 |
|
10 |
p. 525-535 11 p. |
artikel |
44 |
The emerging role of long non-coding RNAs in endometrial cancer
|
Takenaka, Konii |
|
2016 |
|
10 |
p. 445-455 11 p. |
artikel |
45 |
t(9;22)(q34;q11.2) is a recurrent constitutional non-Robertsonian translocation and a rare cytogenetic mimic of chronic myeloid leukemia
|
Czuchlewski, David R. |
|
2011 |
|
10 |
p. 572-576 5 p. |
artikel |
46 |
Translocation t(2;11) is characteristic of collagenous fibroma (desmoplastic fibroblastoma)
|
Nishio, Jun |
|
2011 |
|
10 |
p. 569-571 3 p. |
artikel |