nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An intronic variant in the TP53 gene in a Brazilian woman with breast cancer
|
Lacerda, Leandra Linhares |
|
2005 |
160 |
2 |
p. 160-163 4 p. |
artikel |
2 |
Characterization of ABCG2 gene amplification manifesting as extrachromosomal DNA in mitoxantrone-selected SF295 human glioblastoma cells
|
Rao, V. Koneti |
|
2005 |
160 |
2 |
p. 126-133 8 p. |
artikel |
3 |
Chromosome alterations in colorectal cancer in Thai patients
|
Poeaim, S. |
|
2005 |
160 |
2 |
p. 152-159 8 p. |
artikel |
4 |
Complex CGH alterations on chromosome arm 8p at candidate tumor suppressor gene loci in breast cancer cell lines
|
Venter, Deon J. |
|
2005 |
160 |
2 |
p. 134-140 7 p. |
artikel |
5 |
Deletions of the 3′ BCR and 5′ ABL regions in patients with Philadelphia-positive chronic myeloid leukemia: a one-step process occurring in about 10% of the cases without any evidence of genetic instability in the target cells
|
Fournier, Mickaël |
|
2005 |
160 |
2 |
p. 184-187 4 p. |
artikel |
6 |
Editorial board
|
|
|
2005 |
160 |
2 |
p. CO2- 1 p. |
artikel |
7 |
Gain of 9p due to an unbalanced rearrangement der(9;18): a recurrent clonal abnormality in chronic myeloproliferative disorders
|
Bacher, Ulrike |
|
2005 |
160 |
2 |
p. 179-183 5 p. |
artikel |
8 |
Genetic losses in breast cancer: toward an integrated molecular cytogenetic map
|
Mao, Xin |
|
2005 |
160 |
2 |
p. 141-151 11 p. |
artikel |
9 |
Hereditary breast cancer syndromes in a Turkish population. Results of molecular germline analysis
|
Güran, Şefik |
|
2005 |
160 |
2 |
p. 164-168 5 p. |
artikel |
10 |
Identification of a ring chromosome with spectral karyotyping in a pleural synovial sarcoma
|
Nishio, Jun |
|
2005 |
160 |
2 |
p. 174-178 5 p. |
artikel |
11 |
Losses of 1p and chromosome 14 in renal oncocytomas
|
Füzesi, László |
|
2005 |
160 |
2 |
p. 120-125 6 p. |
artikel |
12 |
No evidence of INI1hSNF5 (SMARCB1) and PARVG point mutations in oligodendroglial neoplasms
|
Alonso, M. Eva |
|
2005 |
160 |
2 |
p. 169-173 5 p. |
artikel |
13 |
Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases
|
Beyer, Valérie |
|
2005 |
160 |
2 |
p. 97-119 23 p. |
artikel |
14 |
Prognostic significance of del(20q) in patients with hematological malignancies
|
Březinová, Jana |
|
2005 |
160 |
2 |
p. 188-192 5 p. |
artikel |
15 |
Table of contents
|
|
|
2005 |
160 |
2 |
p. A1-A2 nvt p. |
artikel |