| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Announcement to contributors
|
|
|
2003
|
146 |
1 |
p. I-
1 p.
|
artikel
|
| 2 |
Cancer Genetics and Cytogenetics
|
|
|
2003
|
146 |
1 |
p. IFC-
1 p.
|
artikel
|
| 3 |
Caspase 3 and 8 deficiency in human neuroblastoma
|
Iolascon, Achille
|
|
2003
|
146 |
1 |
p. 41-47
7 p.
|
artikel
|
| 4 |
Clinicopathologic significance of genetic alterations in hepatocellular carcinoma
|
Pang, A.
|
|
2003
|
146 |
1 |
p. 8-15
8 p.
|
artikel
|
| 5 |
Deletion (6)(p22p25) is a recurrent anomaly of thymoma: report of a second case and review of the literature
|
Herens, Christian
|
|
2003
|
146 |
1 |
p. 66-69
4 p.
|
artikel
|
| 6 |
Detection of amplified oncogenes by genome DNA microarrays in human primary esophageal squamous cell carcinoma: comparison with conventional comparative genomic hybridization analysis
|
Arai, Hiroshi
|
|
2003
|
146 |
1 |
p. 16-21
6 p.
|
artikel
|
| 7 |
Does conventional cytogenetics detect the real frequency of 19q13 aberrations in benign thyroid lesions? A survey of 38 cases
|
Meiboom, Maren
|
|
2003
|
146 |
1 |
p. 70-72
3 p.
|
artikel
|
| 8 |
Genetic and epigenetic alterations in sentinel lymph nodes metastatic lesions compared to their corresponding primary breast tumors
|
Cavalli, Luciane R.
|
|
2003
|
146 |
1 |
p. 33-40
8 p.
|
artikel
|
| 9 |
Identification of germline MSH2 gene mutations in endometrial cancer not fulfilling the new clinical criteria for hereditary nonpolyposis colorectal cancer
|
Banno, Kouji
|
|
2003
|
146 |
1 |
p. 58-65
8 p.
|
artikel
|
| 10 |
Low microsatellite instability and high loss of heterozygosity rates indicate dominant role of the suppressor pathway in squamous cell carcinoma of head and neck and loss of heterozygosity of 11q14.3 correlates with tumor grade
|
Glavač, Damjan
|
|
2003
|
146 |
1 |
p. 27-32
6 p.
|
artikel
|
| 11 |
Molecular cytogenetic characterization of desmoid tumors
|
Brandal, Petter
|
|
2003
|
146 |
1 |
p. 1-7
7 p.
|
artikel
|
| 12 |
Neuroblastoma in a patient with 47, XXX karyotype
|
Gül, Davut
|
|
2003
|
146 |
1 |
p. 84-85
2 p.
|
artikel
|
| 13 |
One allele deletion of the RB1 gene in a case of refractory anemia with del(13)(q12q14): a fluorescence in situ hybridization study of the RB1 gene
|
Nagamura, Fumitaka
|
|
2003
|
146 |
1 |
p. 77-80
4 p.
|
artikel
|
| 14 |
RFP2, c13ORF1, and FAM10A4 are the most likely tumor suppressor gene candidates for B-cell chronic lymphocytic leukemia
|
van Everdink, W.J
|
|
2003
|
146 |
1 |
p. 48-57
10 p.
|
artikel
|
| 15 |
T-cell prolymphocytic leukemia with der(11)t(1;11)(q21;q23) and ATM deficiency
|
Yamaguchi, Mitsuko
|
|
2003
|
146 |
1 |
p. 22-26
5 p.
|
artikel
|
| 16 |
The apolipoprotein E ε4 allele is not a risk factor for Turkish breast cancer patients
|
Yaylim, Ilhan
|
|
2003
|
146 |
1 |
p. 86-87
2 p.
|
artikel
|
| 17 |
Trisomy 8 as the sole chromosomal aberration inmyelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations
|
Heller, Anita
|
|
2003
|
146 |
1 |
p. 81-83
3 p.
|
artikel
|
| 18 |
X chromosome inactivation in cervical cancer patients
|
Kristiansen, Marianne
|
|
2003
|
146 |
1 |
p. 73-76
4 p.
|
artikel
|
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