nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A closer look at Warthin tumors and the t(11;19)
|
Fehr, André |
|
2008 |
180 |
2 |
p. 135-139 5 p. |
artikel |
2 |
A novel MEN1 gene mutation
|
Manzoni, Marco F. |
|
2008 |
180 |
2 |
p. 165-167 3 p. |
artikel |
3 |
Aplastic anemia and Turner syndrome
|
Cuturilo, Goran |
|
2008 |
180 |
2 |
p. 158-159 2 p. |
artikel |
4 |
Basal level micronucleus frequency in stimulated lymphocytes of untreated patients with leukemia
|
Hamurcu, Zuhal |
|
2008 |
180 |
2 |
p. 140-144 5 p. |
artikel |
5 |
Copy number alterations of the H2AFX gene in sporadic breast cancer patients
|
Srivastava, Niloo |
|
2008 |
180 |
2 |
p. 121-128 8 p. |
artikel |
6 |
Does Schistosoma-associated bladder cancer differ from urothelial cancer? Proof from the laboratory and clinic
|
Zaghloul, Mohamed S. |
|
2008 |
180 |
2 |
p. 160-162 3 p. |
artikel |
7 |
Editorial board
|
|
|
2008 |
180 |
2 |
p. IFC- 1 p. |
artikel |
8 |
Karyotypic characterization of infant embryonal rhabdomyosarcoma
|
Muntean, Andrea |
|
2008 |
180 |
2 |
p. 145-148 4 p. |
artikel |
9 |
Late appearance of a Philadelphia chromosome in a patient with therapy-related acute myeloid leukemia and high expression of EVI1
|
Yagyu, Shigeki |
|
2008 |
180 |
2 |
p. 115-120 6 p. |
artikel |
10 |
Molecular cytogenetic findings in a three-way novel variant of t(1;8;21)(p35;q22;q22): a unique relocation of the AML1/ETO fusion gene 1p35 in AML-M2
|
Ahmad, Firoz |
|
2008 |
180 |
2 |
p. 153-157 5 p. |
artikel |
11 |
Multiple copies of RUNX1: description of 14 new patients, follow-up, and a review of the literature
|
Pérez-Vera, Patricia |
|
2008 |
180 |
2 |
p. 129-134 6 p. |
artikel |
12 |
RUNX1 rearrangements in acute myeloblastic leukemia relapsing after hematopoietic stem cell transplantation
|
Nadal, Nathalie |
|
2008 |
180 |
2 |
p. 168-169 2 p. |
artikel |
13 |
Small marker chromosome and monosomy 7 in a pediatric patient with MDS
|
Zámečníkova, Adriana |
|
2008 |
180 |
2 |
p. 163-164 2 p. |
artikel |
14 |
Somatic mutations in mismatch repair genes in sporadic gastric carcinomas are not a cause but a consequence of the mutator phenotype
|
Pinto, Mafalda |
|
2008 |
180 |
2 |
p. 110-114 5 p. |
artikel |
15 |
Specific clones of spontaneously evolving karyotypes generate individuality of cancers
|
Fabarius, Alice |
|
2008 |
180 |
2 |
p. 89-99 11 p. |
artikel |
16 |
Table of contents
|
|
|
2008 |
180 |
2 |
p. A1-A2 nvt p. |
artikel |
17 |
The UOK 257 cell line: a novel model for studies of the human Birt–Hogg–Dubé gene pathway
|
Yang, Youfeng |
|
2008 |
180 |
2 |
p. 100-109 10 p. |
artikel |
18 |
Translocation (2;11)(q37;q23) in therapy-related myelodysplastic syndrome after treatment for acute promyelocytic leukemia
|
Snijder, Simone |
|
2008 |
180 |
2 |
p. 149-152 4 p. |
artikel |