| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of adult acute myelocytic leukemia (M5a) with a near-tetraploid karyotype characterized by monosomies 5 and 16
|
Gozzetti, Alessandro
|
|
2004
|
150 |
1 |
p. 88-89
2 p.
|
artikel
|
| 2 |
A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome
|
Zagaria, Antonella
|
|
2004
|
150 |
1 |
p. 81-85
5 p.
|
artikel
|
| 3 |
Analysis of human papillomavirus prevalence and TP53 polymorphism in head and neck squamous cell carcinomas
|
Cortezzi, Sylvia Sanches
|
|
2004
|
150 |
1 |
p. 44-49
6 p.
|
artikel
|
| 4 |
A t(20;21)(q12;q22.3) in a patient with chronic myelocytic leukemia in blastic phase
|
Gozzetti, Alessandro
|
|
2004
|
150 |
1 |
p. 90-91
2 p.
|
artikel
|
| 5 |
Characterization of large chromosome markers in a malignant fibrous histiocytoma by spectral karyotyping, comparative genomic hybridization (CGH), and array CGH
|
Weng, Wen-Hui
|
|
2004
|
150 |
1 |
p. 27-32
6 p.
|
artikel
|
| 6 |
Clonal chromosome abnormalities in a plexiform cellular schwannoma
|
Joste, Nancy E
|
|
2004
|
150 |
1 |
p. 73-77
5 p.
|
artikel
|
| 7 |
Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma
|
Amare (Kadam), P.S
|
|
2004
|
150 |
1 |
p. 33-43
11 p.
|
artikel
|
| 8 |
Detection of inv(16)(p13q22) by means of chromosome painting with a 16q-specific probe
|
Li, Ming
|
|
2004
|
150 |
1 |
p. 86-87
2 p.
|
artikel
|
| 9 |
Detection of micronuclei formation and nuclear anomalies in regenerative nodules of human cirrhotic livers and relationship to hepatocellular carcinoma
|
de Almeida, Terezinha M.B
|
|
2004
|
150 |
1 |
p. 16-21
6 p.
|
artikel
|
| 10 |
Detection of t(14;18) in follicular lymphoma by dual-color fluorescence in situ hybridization on paraffin-embedded tissue sections
|
Matsumoto, Yosuke
|
|
2004
|
150 |
1 |
p. 22-26
5 p.
|
artikel
|
| 11 |
Editorial Board
|
|
|
2004
|
150 |
1 |
p. IFC-
1 p.
|
artikel
|
| 12 |
Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences
|
Canto, Patricia
|
|
2004
|
150 |
1 |
p. 70-72
3 p.
|
artikel
|
| 13 |
High frequency of genomic instability in Ewing family of tumors
|
Ohali, Anat
|
|
2004
|
150 |
1 |
p. 50-56
7 p.
|
artikel
|
| 14 |
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma
|
Höglund, Mattias
|
|
2004
|
150 |
1 |
p. 1-8
8 p.
|
artikel
|
| 15 |
T-cell acute lymphoblastic leukemia with add(1)(p36) and del(12)(p11) following acute myelocytic leukemia with partial deletion of 9p
|
Yoshida, Chikashi
|
|
2004
|
150 |
1 |
p. 62-65
4 p.
|
artikel
|
| 16 |
The occurrence of chromosome segregational defects is an intrinsic and heritable property of oral squamous cell carcinoma cell lines
|
Reing, Janet E
|
|
2004
|
150 |
1 |
p. 57-61
5 p.
|
artikel
|
| 17 |
Translocation (11;13)(q23;q14) as the sole abnormality in a childhood de novo acute myelocytic leukemia
|
Tsang, Kam Sze
|
|
2004
|
150 |
1 |
p. 78-80
3 p.
|
artikel
|
| 18 |
Trisomy 4 as the sole karyotypic abnormality in a case of acute biphenotypic leukemia with T-lineage markers in minimally differentiated acute myelocytic leukemia
|
Al-Qurashi, Fat-hia
|
|
2004
|
150 |
1 |
p. 66-69
4 p.
|
artikel
|
| 19 |
Wilms tumors develop through two distinct karyotypic pathways
|
Höglund, Mattias
|
|
2004
|
150 |
1 |
p. 9-15
7 p.
|
artikel
|
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