| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acquired gain of an X chromosome as the sole abnormality in the blast crisis of chronic neutrophilic leukemia
|
Yamamoto, Katsuya
|
|
2002
|
134 |
1 |
p. 84-87
4 p.
|
artikel
|
| 2 |
Adrenal myelolipoma with translocation (3;21)(q25;p11)
|
Chang, Kong-Chao
|
|
2002
|
134 |
1 |
p. 77-80
4 p.
|
artikel
|
| 3 |
Alterations in the suppressor gene PPP2R1B in parathyroid hyperplasias and adenomas
|
Hemmer, Samuli
|
|
2002
|
134 |
1 |
p. 13-17
5 p.
|
artikel
|
| 4 |
Analysis of the NF2 gene in oligodendrogliomas and ependymomas
|
Alonso, M.Eva
|
|
2002
|
134 |
1 |
p. 1-5
5 p.
|
artikel
|
| 5 |
Characterization of a complex chromosome rearrangement involving 6q in a melanoma cell line by chromosome microdissection
|
Guan, Xin-Yuan
|
|
2002
|
134 |
1 |
p. 65-70
6 p.
|
artikel
|
| 6 |
Chromosome changes in sarcomatoid renal carcinomas are different from those in renal cell carcinomas
|
Dal Cin, Paola
|
|
2002
|
134 |
1 |
p. 38-40
3 p.
|
artikel
|
| 7 |
Cytogenetic aberrations and heterogeneity of mutations in repeat-containing genes in a colon carcinoma from a patient with hereditary nonpolyposis colorectal cancer
|
Planck, Maria
|
|
2002
|
134 |
1 |
p. 46-54
9 p.
|
artikel
|
| 8 |
Cytogenetic and molecular analysis of early stage renal cell carcinomas in a family with a translocation (2;3)(q35;q21)
|
Bodmer, Danielle
|
|
2002
|
134 |
1 |
p. 6-12
7 p.
|
artikel
|
| 9 |
Elevated frequency of ATM gene missense mutations in breast cancer relative to ethnically matched controls
|
Sommer, Steve S.
|
|
2002
|
134 |
1 |
p. 25-32
8 p.
|
artikel
|
| 10 |
Erratum
|
|
|
2002
|
134 |
1 |
p. 91-
1 p.
|
artikel
|
| 11 |
Evaluation of ETF1/eRF1, mapping to 5q31, as a candidate myeloid tumor suppressor gene
|
Dubourg, Christèle
|
|
2002
|
134 |
1 |
p. 33-37
5 p.
|
artikel
|
| 12 |
Fluorescence in situ hybridization improves cytogenetic results in the analysis of hepatoblastoma
|
Sainati, L
|
|
2002
|
134 |
1 |
p. 18-20
3 p.
|
artikel
|
| 13 |
Genome-wide survey for chromosomal imbalances in ganglioglioma using comparative genomic hybridization
|
Yin, Xiao-Lu
|
|
2002
|
134 |
1 |
p. 71-76
6 p.
|
artikel
|
| 14 |
New cytogenetic variant, insertion (15;17)(q22;q12q21), in an adolescent with acute promyelocytic leukemia
|
Rolston, Raj
|
|
2002
|
134 |
1 |
p. 55-59
5 p.
|
artikel
|
| 15 |
Numerical aberrations of chromosome 9 in bladder cancer.
|
Tsukamoto, Manabu
|
|
2002
|
134 |
1 |
p. 41-45
5 p.
|
artikel
|
| 16 |
Significance of cytogenetic and fluorescence in situ hybridization analysis in evaluating antichronic myeloid leukemia efficacy of different immune effector cells
|
Tong, Chun-Rong
|
|
2002
|
134 |
1 |
p. 21-24
4 p.
|
artikel
|
| 17 |
Tetrasomy 21 as a sole chromosome abnormality in acute myeloid leukemia
|
Ohsaka, Akimichi
|
|
2002
|
134 |
1 |
p. 60-64
5 p.
|
artikel
|
| 18 |
Translocation (1;19)(q21;q13.3) is a recurrent reciprocal translocation in meningioma
|
Sawyer, Jeffrey R.
|
|
2002
|
134 |
1 |
p. 88-90
3 p.
|
artikel
|
| 19 |
Trisomy 10 and acute myeloid leukemia
|
Czepulkowski, Barbara
|
|
2002
|
134 |
1 |
p. 81-83
3 p.
|
artikel
|
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