| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia
|
Park, Tae Sung
|
|
2009
|
195 |
1 |
p. 94-95
2 p.
|
artikel
|
| 2 |
Cytogenetic, fluorescence in situ hybridization, and molecular characterization of chronic myeloid leukemia in chronic phase with four BCR/ABL1 fusion signals: a case report
|
Vargas, Maria Teresa
|
|
2009
|
195 |
1 |
p. 71-74
4 p.
|
artikel
|
| 3 |
Cytogenetic study of a pulmonary sclerosing hemangioma
|
Pareja, María J.
|
|
2009
|
195 |
1 |
p. 80-84
5 p.
|
artikel
|
| 4 |
Detailed cytogenetic and array analysis of pediatric primitive sarcomas reveals a recurrent CIC–DUX4 fusion gene event
|
Yoshimoto, Maisa
|
|
2009
|
195 |
1 |
p. 1-11
11 p.
|
artikel
|
| 5 |
Detection of chromosomal abnormalities associated with chronic lymphocytic leukemia: what is the best method?
|
el-Taweel, Maha
|
|
2009
|
195 |
1 |
p. 37-42
6 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2009
|
195 |
1 |
p. IFC-
1 p.
|
artikel
|
| 7 |
Establishment and conventional cytogenetic characterization of three gastric cancer cell lines
|
Leal, Mariana Ferreira
|
|
2009
|
195 |
1 |
p. 85-91
7 p.
|
artikel
|
| 8 |
FGFR3 amplification in the absence of IGH@–FGFR3 fusion t(4;14) in myeloma
|
Quintero-Rivera, Fabiola
|
|
2009
|
195 |
1 |
p. 92-93
2 p.
|
artikel
|
| 9 |
Fusion of EWSR1 with the DUX4 facioscapulohumeral muscular dystrophy region resulting from t(4;22)(q35;q12) in a case of embryonal rhabdomyosarcoma
|
Sirvent, Nicolas
|
|
2009
|
195 |
1 |
p. 12-18
7 p.
|
artikel
|
| 10 |
Germline mutations in MEN1 and BRCA1 genes in a woman with familial multiple endocrine neoplasia type 1 and inherited breast–ovarian cancer syndromes: a case report
|
Papi, Laura
|
|
2009
|
195 |
1 |
p. 75-79
5 p.
|
artikel
|
| 11 |
HMGA2–NFIB fusion in a pediatric intramuscular lipoma: a novel case of NFIB alteration in a large deep-seated adipocytic tumor
|
Pierron, Anne
|
|
2009
|
195 |
1 |
p. 66-70
5 p.
|
artikel
|
| 12 |
Homozygous deletion of CDKN2A (p16, p14) and CDKN2B (p15) genes is a poor prognostic factor in adult but not in childhood B-lineage acute lymphoblastic leukemia: a comparative deletion and hypermethylation study
|
Kim, Miyoung
|
|
2009
|
195 |
1 |
p. 59-65
7 p.
|
artikel
|
| 13 |
Novel SYT–SSX fusion transcript variants in synovial sarcoma
|
Dimitriadis, Euthimios
|
|
2009
|
195 |
1 |
p. 54-58
5 p.
|
artikel
|
| 14 |
Polymorphisms in one-carbon metabolism pathway genes and risk for bladder cancer in a Tunisian population
|
Rouissi, Kamel
|
|
2009
|
195 |
1 |
p. 43-53
11 p.
|
artikel
|
| 15 |
Screening of TERC gene amplification as an additional genetic diagnostic test in detection of cervical preneoplastic lesions
|
Kokalj-Vokač, Nadja
|
|
2009
|
195 |
1 |
p. 19-22
4 p.
|
artikel
|
| 16 |
Table of Contents
|
|
|
2009
|
195 |
1 |
p. A1-A2
nvt p.
|
artikel
|
| 17 |
Telomere aggregate formation in placenta specimens of pregnancies complicated with pre-eclampsia
|
Sukenik-Halevy, Rivka
|
|
2009
|
195 |
1 |
p. 27-30
4 p.
|
artikel
|
| 18 |
Telomere aggregates in trisomy 21 amniocytes
|
Hadi, Efrat
|
|
2009
|
195 |
1 |
p. 23-26
4 p.
|
artikel
|
| 19 |
TP53 R72P and MDM2 SNP309 polymorphisms in modification of childhood acute lymphoblastic leukemia susceptibility
|
Do, Thuy N.
|
|
2009
|
195 |
1 |
p. 31-36
6 p.
|
artikel
|
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