no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
A diminutive chromosome 21 centromere in acute lymphoblastic leukemia
|
Roberts, Kathryn A. |
|
2006 |
167 |
1 |
p. 78-81 4 p. |
article |
2 |
Allele-specific loss of heterozygosity in multiple colorectal adenomas: toward an integrated molecular cytogenetic map II
|
Mao, Xin |
|
2006 |
167 |
1 |
p. 1-14 14 p. |
article |
3 |
Allelic imbalance of HER2 variant in sporadic breast and ovarian cancer
|
Puputti, Marjut |
|
2006 |
167 |
1 |
p. 32-38 7 p. |
article |
4 |
A molecular study of first and second RB1 mutational hits in retinoblastoma patients
|
de Andrade, Ana Flávia Belchior |
|
2006 |
167 |
1 |
p. 43-46 4 p. |
article |
5 |
A suggested protocol for obtaining high-quality skin metaphases from primary cutaneous T-cell lymphoma
|
Chevret, Edith |
|
2006 |
167 |
1 |
p. 89-91 3 p. |
article |
6 |
A variant of the SYT-SSX2 fusion gene in a case of synovial sarcoma
|
Otsuka, Seiji |
|
2006 |
167 |
1 |
p. 82-88 7 p. |
article |
7 |
Chromosomal aberrations in 130 patients with multiple myeloma studied by interphase FISH: diagnostic and prognostic relevance
|
Schmidt-Wolf, I.G.H. |
|
2006 |
167 |
1 |
p. 20-25 6 p. |
article |
8 |
Delineation by molecular cytogenetics of 5q deletion breakpoints in myelodyplastic syndromes and acute myeloid leukemia
|
Royer-Pokora, Brigitte |
|
2006 |
167 |
1 |
p. 66-69 4 p. |
article |
9 |
Detection of abnormalities of PRV-1, TPO, and c-MPL genes detected by fluorescence in situ hybridization in essential thrombocythemia
|
Puigdecanet, Eulàlia |
|
2006 |
167 |
1 |
p. 39-42 4 p. |
article |
10 |
Editorial board
|
|
|
2006 |
167 |
1 |
p. CO2- 1 p. |
article |
11 |
Emergence of chronic myelogenous leukemia in a patient with primary thrombocythemia and absence of BCR/ABL rearrangement
|
Cesar, Jesus M. |
|
2006 |
167 |
1 |
p. 74-77 4 p. |
article |
12 |
Erratum
|
|
|
2006 |
167 |
1 |
p. 95- 1 p. |
article |
13 |
Evaluation of microsatellite amplifications at chromosomal locus 3q26 as surrogate marker for premalignant changes in mucosa surrounding head and neck squamous cell carcinoma
|
Brieger, Jürgen |
|
2006 |
167 |
1 |
p. 26-31 6 p. |
article |
14 |
Favorable outcome of triploid neuroblastomas: a contribution to the special oncogenesis of neuroblastoma
|
Spitz, Ruediger |
|
2006 |
167 |
1 |
p. 51-56 6 p. |
article |
15 |
Forthcoming events
|
|
|
2006 |
167 |
1 |
p. 96- 1 p. |
article |
16 |
Genome-wide semiquantitative microsatellite analysis of human hepatocellular carcinoma: discrete mapping of smallest region of overlap of recurrent chromosomal gains and losses
|
Nishimura, Takafumi |
|
2006 |
167 |
1 |
p. 57-65 9 p. |
article |
17 |
Juvenile myelomonocytic leukemia in a child with Crohn disease
|
Oliver, Jeffrey W. |
|
2006 |
167 |
1 |
p. 70-73 4 p. |
article |
18 |
Myelodysplastic syndromes with isolated deletion of the long arm of the chromosome X as a sole cytogenetic change
|
Olshanskaya, Yulia V. |
|
2006 |
167 |
1 |
p. 47-50 4 p. |
article |
19 |
Table of contents
|
|
|
2006 |
167 |
1 |
p. A1-A2 nvt p. |
article |
20 |
Transitional cell bladder tumor: predicting recurrence and progression by analysis of microsatellite loss of heterozygosity in urine sediment and tumor tissue
|
Fornari, Delfina |
|
2006 |
167 |
1 |
p. 15-19 5 p. |
article |
21 |
Translocations of 17q21∼qter in neuroblastoma cell lines infrequently include the topoisomerase IIα gene
|
Yoon, K. Jin |
|
2006 |
167 |
1 |
p. 92-94 3 p. |
article |