| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A gene dosage effect is responsible for high overexpression of the MUC1 gene observed in human breast tumors
|
Bièche, Ivan
|
|
1997
|
98 |
1 |
p. 75-80
6 p.
|
artikel
|
| 2 |
Allelic imbalance mapping of chromosome 16 shows two regions of common deletion in prostate adenocarcinoma
|
Godfrey, Tony E
|
|
1997
|
98 |
1 |
p. 36-42
7 p.
|
artikel
|
| 3 |
Analysis of the p16INK4 and TP53 tumor suppressor genes in bone sarcoma pediatric patients
|
Patiño-García, A.
|
|
1997
|
98 |
1 |
p. 50-55
6 p.
|
artikel
|
| 4 |
Announcement
|
|
|
1997
|
98 |
1 |
p. i-iii
nvt p.
|
artikel
|
| 5 |
Assessment of chromosome 3 copy number in ocular melanoma using fluorescence in situ hybridization
|
McNamara, Morgan
|
|
1997
|
98 |
1 |
p. 4-8
5 p.
|
artikel
|
| 6 |
A third case of a low-grade endometrial stromal sarcoma with a t(7;17)(p14∼21;q11.2∼21)
|
Hennig, Yvonne
|
|
1997
|
98 |
1 |
p. 84-86
3 p.
|
artikel
|
| 7 |
Complementation analysis of testis tumor cells
|
Wang, Xianghong
|
|
1997
|
98 |
1 |
p. 56-62
7 p.
|
artikel
|
| 8 |
Detection of a dup(17q) and inv(16) by fluorescence in situ hybridization in acute myelomonocytic leukemia
|
Koo, SunHoe
|
|
1997
|
98 |
1 |
p. 87-89
3 p.
|
artikel
|
| 9 |
Editorial Board
|
|
|
1997
|
98 |
1 |
p. IFC-
1 p.
|
artikel
|
| 10 |
Erratum
|
|
|
1997
|
98 |
1 |
p. 92-
1 p.
|
artikel
|
| 11 |
Fluorescence in situ hybridization assessment of the telomeric regions of jumping translocations in a case of aggressive B-cell non-Hodgkin lymphoma
|
Gray, Brian A.
|
|
1997
|
98 |
1 |
p. 20-27
8 p.
|
artikel
|
| 12 |
Fluorescence in situ hybridization of old G-banded and mounted chromosome preparations
|
Gerdes, Anne-Marie
|
|
1997
|
98 |
1 |
p. 9-15
7 p.
|
artikel
|
| 13 |
Frequent allelic losses of 9p21 markers and low incidence of mutations at p16(CDKN2) gene in non-Hodgkin lymphomas of B-cell lineage
|
Fernández-Piqueras, José
|
|
1997
|
98 |
1 |
p. 63-68
6 p.
|
artikel
|
| 14 |
Hypermethylation in the retinoblastoma gene is associated with unilateral, sporadic retinoblastoma
|
Ohtani-Fujita, Naoko
|
|
1997
|
98 |
1 |
p. 43-49
7 p.
|
artikel
|
| 15 |
Karyotypic and clinical progression of ANLL in a patient with constitutional der(15;21)(q10;q10)
|
Zámečniková, Adriana
|
|
1997
|
98 |
1 |
p. 81-83
3 p.
|
artikel
|
| 16 |
Myelodysplasia with der(1;7)(q10;p10) discovered after an episode of bacterial lymphangitis in a twenty-three-year-old man
|
Bauduer, Frederic
|
|
1997
|
98 |
1 |
p. 90-91
2 p.
|
artikel
|
| 17 |
p53 loss and point mutations are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis
|
Stuppia, Liborio
|
|
1997
|
98 |
1 |
p. 28-35
8 p.
|
artikel
|
| 18 |
Some observations on fluorescence in situ hybridization evaluation of chronic myelocytic leukemia
|
Chen, Zhong
|
|
1997
|
98 |
1 |
p. 1-3
3 p.
|
artikel
|
| 19 |
The del(7q) subgroup in uterine leiomyomata: Genetic and biologic characteristics
|
Polly Xing, Y.
|
|
1997
|
98 |
1 |
p. 69-74
6 p.
|
artikel
|
| 20 |
Unbalanced X;autosome translocation (X;18)(q13;p11) in a case of aggressive natural killer non-Hodgkin lymphoma
|
Callet-Bauchu, Evelyne
|
|
1997
|
98 |
1 |
p. 16-19
4 p.
|
artikel
|
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