| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Amplification of BCR–ABL and t(3;21) in a patient with blast crisis of chronic myelogenous leukemia
|
Phan, Chin-Lee
|
|
2008
|
180 |
1 |
p. 60-64
5 p.
|
artikel
|
| 2 |
A rare tumor and an ethical dilemma in a family with a germline TP53 mutation
|
Prochazkova, Kamila
|
|
2008
|
180 |
1 |
p. 65-69
5 p.
|
artikel
|
| 3 |
Characterization of complex chromosome aberrations in a recurrent meningioma combining standard cytogenetic and array comparative genomic hybridization techniques
|
Woo, Kwang-Sook
|
|
2008
|
180 |
1 |
p. 56-59
4 p.
|
artikel
|
| 4 |
Concomitant chronic myeloid leukemia and chronic lymphocytic leukemia: a different clonal origin shown by molecular cytogenetics
|
Gozzetti, Alessandro
|
|
2008
|
180 |
1 |
p. 83-84
2 p.
|
artikel
|
| 5 |
CREB3L4, INTS3, and SNAPAP are targets for the 1q21 amplicon frequently detected in hepatocellular carcinoma
|
Inagaki, Yoshikazu
|
|
2008
|
180 |
1 |
p. 30-36
7 p.
|
artikel
|
| 6 |
Determination of ancestral allele for possible human cancer-associated polymorphisms
|
Maruta, Yuichi
|
|
2008
|
180 |
1 |
p. 24-29
6 p.
|
artikel
|
| 7 |
Disruption of the ETV6 gene as a consequence of a rare translocation (12;12)(p13;q13) in treatment-induced acute myeloid leukemia after breast cancer
|
Manola, Kalliopi N.
|
|
2008
|
180 |
1 |
p. 37-42
6 p.
|
artikel
|
| 8 |
Editorial board
|
|
|
2008
|
180 |
1 |
p. IFC-
1 p.
|
artikel
|
| 9 |
FAS −1377 G/A polymorphism and the risk of lymph node metastasis in cervical cancer
|
Kang, Sokbom
|
|
2008
|
180 |
1 |
p. 1-5
5 p.
|
artikel
|
| 10 |
Fusion of the COL1A1 and USP6 genes in a benign bone tumor
|
Panagopoulos, Ioannis
|
|
2008
|
180 |
1 |
p. 70-73
4 p.
|
artikel
|
| 11 |
How early to test for a cancer-causing germline mutation
|
Lynch, Henry T.
|
|
2008
|
180 |
1 |
p. 87-88
2 p.
|
artikel
|
| 12 |
Identification of polymorphisms in the XIAP gene and analysis of association with lung cancer risk in a Korean population
|
Kang, Hyo-Gyoung
|
|
2008
|
180 |
1 |
p. 6-13
8 p.
|
artikel
|
| 13 |
Loss of the extra chromosome 21 in a patient with Down syndrome and myelodysplasia
|
Tan, Daryl
|
|
2008
|
180 |
1 |
p. 79-82
4 p.
|
artikel
|
| 14 |
Methylation of PTCH1, the Patched-1 gene, in a panel of primary medulloblastomas
|
Pritchard, Joel I.
|
|
2008
|
180 |
1 |
p. 47-50
4 p.
|
artikel
|
| 15 |
Mutations of GATA1, FLT3, MLL-partial tandem duplication, NRAS, and RUNX1 genes are not found in a 7-year-old Down syndrome patient with acute myeloid leukemia (FAB-M2) having a good prognosis
|
Kawamura, Machiko
|
|
2008
|
180 |
1 |
p. 74-78
5 p.
|
artikel
|
| 16 |
NUP98–NSD1 fusion by insertion in acute myeloblastic leukemia
|
Petit, Arnaud
|
|
2008
|
180 |
1 |
p. 43-46
4 p.
|
artikel
|
| 17 |
Polycythemia vera transforming to acute myeloid leukemia and complex abnormalities including 9p homogeneously staining region with amplification of MLLT3, JMJD2C, JAK2, and SMARCA2
|
Hélias, Catherine
|
|
2008
|
180 |
1 |
p. 51-55
5 p.
|
artikel
|
| 18 |
Random aneuploidy in chronic hepatitis C patients
|
Goldberg-Bittman, Lilach
|
|
2008
|
180 |
1 |
p. 20-23
4 p.
|
artikel
|
| 19 |
Table of contents
|
|
|
2008
|
180 |
1 |
p. A1-A2
nvt p.
|
artikel
|
| 20 |
TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas
|
Lima-Ramos, Vítor
|
|
2008
|
180 |
1 |
p. 14-19
6 p.
|
artikel
|
| 21 |
Translocation (8;21)(q22;q22) without rearrangement of RUNX1 and RUNX1T1 genes in a patient with refractory anemia with excess of blasts
|
Aguilar, Alberto
|
|
2008
|
180 |
1 |
p. 85-86
2 p.
|
artikel
|
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