| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aberrations of chromosome 8 in 16 breast cancer cell lines by comparative genomic hybridization, fluorescence in situ hybridization, and spectral karyotyping
|
Rummukainen, Jaana
|
|
2001
|
126 |
1 |
p. 1-7
7 p.
|
artikel
|
| 2 |
Additional t(11;17)(q23;q21) in a patient with Philadelphia-positive mixed lineage antigen-expressing leukemia
|
Nishii, Kazuhiro
|
|
2001
|
126 |
1 |
p. 8-12
5 p.
|
artikel
|
| 3 |
Chromosomal analyses of 52 cases of follicular lymphoma with t(14;18), including blastic/blastoid variant
|
Mohamed, Anwar N
|
|
2001
|
126 |
1 |
p. 45-51
7 p.
|
artikel
|
| 4 |
Co-existence of alternative forms of 8q gain in cytogenetic clones of three patients with acute myeloid leukemia, pointing to 8q22∼8qter as a region of biologic significance
|
Batanian, Jacqueline R
|
|
2001
|
126 |
1 |
p. 20-25
6 p.
|
artikel
|
| 5 |
Comparative genomic hybridization analysis of nasopharygeal carcinoma:
|
Chien, Gary
|
|
2001
|
126 |
1 |
p. 63-67
5 p.
|
artikel
|
| 6 |
Correlation between centrosome abnormalities and chromosomal instability in human pancreatic cancer cells
|
Sato, Norihiro
|
|
2001
|
126 |
1 |
p. 13-19
7 p.
|
artikel
|
| 7 |
Cytogenetic instability, predominantly involving chromosome 1, is characteristic of elastofibroma
|
McComb, Erin N
|
|
2001
|
126 |
1 |
p. 68-72
5 p.
|
artikel
|
| 8 |
DNA amplification and chromosomal translocations are accompanied by chromosomal instability:
|
Tsushimi, Takaaki
|
|
2001
|
126 |
1 |
p. 34-38
5 p.
|
artikel
|
| 9 |
Fanconi anemia
|
Pearson, Thomas
|
|
2001
|
126 |
1 |
p. 52-55
4 p.
|
artikel
|
| 10 |
Low incidence of TEL/AML1 fusion and TEL deletion in Korean childhood acute leukemia by extra-signal fluorescence in situ hybridization
|
Park, Kyoung Un
|
|
2001
|
126 |
1 |
p. 73-77
5 p.
|
artikel
|
| 11 |
Mapping the chromosome 16 cadherin gene cluster to a minimal deleted region in ductal breast cancer
|
Chalmers, I.Jennifer
|
|
2001
|
126 |
1 |
p. 39-44
6 p.
|
artikel
|
| 12 |
No evidence for deletions of the NBS1 gene in lymphomas
|
Stumm, Markus
|
|
2001
|
126 |
1 |
p. 60-62
3 p.
|
artikel
|
| 13 |
No increased frequency of trisomies 8 and 9 by fluorescence in situ hybridization in untreated patients with essential thrombocythemia
|
Swolin, Birgitta
|
|
2001
|
126 |
1 |
p. 56-59
4 p.
|
artikel
|
| 14 |
The application of comparative genomic hybridization as an additional tool in the chromosome analysis of acute myeloid leukemia and myelodysplastic syndromes
|
Kim, Mee Hye
|
|
2001
|
126 |
1 |
p. 26-33
8 p.
|
artikel
|
| 15 |
Trisomy 21 and isodicentric chromosome 21 in Kostmann syndrome following treatment with G-CSF
|
Roland, Birgitte
|
|
2001
|
126 |
1 |
p. 78-80
3 p.
|
artikel
|
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