nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A combination of molecular cytogenetic analyses reveals complex genetic alterations in conventional renal cell carcinoma
|
Strefford, Jon C. |
|
2005 |
159 |
1 |
p. 1-9 9 p. |
artikel |
2 |
Acquisition of a Ph chromosome with minor BCR/ABL fusion in treatment-related myelodysplastic syndrome with chromosome 7 abnormalities in a patient treated for Hodgkin disease
|
Kneller, Abraham |
|
2005 |
159 |
1 |
p. 58-62 5 p. |
artikel |
3 |
A new variant t(6;15;17)(q25;q22;q21) in acute promyelocytic leukemia: fluorescence in situ hybridization confirmation
|
Eclache, Virginie |
|
2005 |
159 |
1 |
p. 69-73 5 p. |
artikel |
4 |
Association between the stages of cervical cancer and chromosome 1 aneusomy
|
Cortés-Gutiérrez, Elva I. |
|
2005 |
159 |
1 |
p. 44-47 4 p. |
artikel |
5 |
Association of functional polymorphisms of SLC11A1 with risk of esophageal cancer in the South African Colored population
|
Zaahl, Monique G. |
|
2005 |
159 |
1 |
p. 48-52 5 p. |
artikel |
6 |
AURKA amplification, chromosome instability, and centrosome abnormality in human pancreatic carcinoma cells
|
Zhu, Jijiang |
|
2005 |
159 |
1 |
p. 10-17 8 p. |
artikel |
7 |
A variant t(8;10;21) in a patient with pathological features mimicking atypical chronic myeloid leukemia
|
Lee, Jiyun |
|
2005 |
159 |
1 |
p. 79-83 5 p. |
artikel |
8 |
Burkitt-type acute leukemia in a patient with B-prolymphocytic leukemia: evidence for a common origin
|
Nguyen-Khac, Florence |
|
2005 |
159 |
1 |
p. 74-78 5 p. |
artikel |
9 |
Copy number gains on 22q13 in adenoid cystic carcinoma of the salivary gland revealed by comparative genomic hybridization and tissue microarray analysis
|
Freier, Kolja |
|
2005 |
159 |
1 |
p. 89-95 7 p. |
artikel |
10 |
Cytogenetically unrelated clones in different histologic components of a Wilms tumor
|
Dolan, Michelle |
|
2005 |
159 |
1 |
p. 63-68 6 p. |
artikel |
11 |
Editorial board
|
|
|
2005 |
159 |
1 |
p. IFC- 1 p. |
artikel |
12 |
Evidence for telomeric fusions as a mechanism for recurring structural aberrations of chromosome 11 in giant cell tumor of bone
|
Sawyer, Jeffrey R. |
|
2005 |
159 |
1 |
p. 32-36 5 p. |
artikel |
13 |
Frequent allelic loss of 21q11.1∼q21.1 region in advanced stage oral squamous cell carcinoma
|
Chen, Lan |
|
2005 |
159 |
1 |
p. 37-43 7 p. |
artikel |
14 |
Genetic changes in localized prostate cancer of Japanese patients shown by comparative genomic hybridization
|
Kasahara, Kotaro |
|
2005 |
159 |
1 |
p. 84-88 5 p. |
artikel |
15 |
Microarray-based comparative genomic hybridization of pheochromocytoma cell lines from neurofibromatosis knockout mice reveals genetic alterations similar to those in human pheochromocytomas
|
Powers, James F. |
|
2005 |
159 |
1 |
p. 27-31 5 p. |
artikel |
16 |
Molecular characterization of a consistent 4.5-megabase deletion at 4q28 in prostate cancer cells
|
Matsui, Sei-Ichi |
|
2005 |
159 |
1 |
p. 18-26 9 p. |
artikel |
17 |
Progress in concurrent analysis of loss of heterozygosity and comparative genomic hybridization utilizing high density single nucleotide polymorphism arrays
|
Zhou, Xiaofeng |
|
2005 |
159 |
1 |
p. 53-57 5 p. |
artikel |
18 |
Table of contents
|
|
|
2005 |
159 |
1 |
p. A1-A2 nvt p. |
artikel |
19 |
Variant translocation t(2;21;8)(q36;q22;q22) with RUNX1/CBFA2T1 (AML1/ETO) transcript in a case of acute myelogenous leukemia
|
Hsiao, Hui-Hua |
|
2005 |
159 |
1 |
p. 96-97 2 p. |
artikel |