| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A microsatellite within the MUC1 locus at 1q21 is altered in the neoplastic cells of breast cancer patients
|
Waltz, Margaret R.
|
|
1998
|
100 |
1 |
p. 63-67
5 p.
|
artikel
|
| 2 |
Announcements
|
|
|
1998
|
100 |
1 |
p. i-ii
nvt p.
|
artikel
|
| 3 |
A novel BRCA1 mutation in an identical twin pair with similar clinical histories
|
Miesfeldt, Susan
|
|
1998
|
100 |
1 |
p. 43-48
6 p.
|
artikel
|
| 4 |
A novel myeloid cell line, Marimo, derived from therapy-related acute myeloid leukemia during treatment of essential thrombocythemia: Consistent chromosomal abnormalities and temporary C-MYC gene amplification
|
Yoshida, Hitoshi
|
|
1998
|
100 |
1 |
p. 21-24
4 p.
|
artikel
|
| 5 |
Comparative genomic hybridization study on pooled DNAs from tumors of one clinical-pathological entity
|
Knuutila, S
|
|
1998
|
100 |
1 |
p. 25-30
6 p.
|
artikel
|
| 6 |
Cytogenetic analysis of four angiosarcomas from deep and superficial soft tissue
|
Schuborg, Claes
|
|
1998
|
100 |
1 |
p. 52-56
5 p.
|
artikel
|
| 7 |
De novo AML with trilineage myelodysplasia and a novel t(11;12)(p15;q13)
|
Wong, K.F
|
|
1998
|
100 |
1 |
p. 49-51
3 p.
|
artikel
|
| 8 |
Development of myeloma and secondary myelodysplastic syndrome from a common clone
|
Schmetzer, Helga M
|
|
1998
|
100 |
1 |
p. 31-35
5 p.
|
artikel
|
| 9 |
Editorial Board
|
|
|
1998
|
100 |
1 |
p. IFC-
1 p.
|
artikel
|
| 10 |
Enhanced expression in seminoma of human zinc finger genes located on chromosome 19
|
Ogawa, Takehiko
|
|
1998
|
100 |
1 |
p. 36-42
7 p.
|
artikel
|
| 11 |
Gliomas in families: Chromosomal analysis by comparative genomic hybridization
|
Patel, Atul
|
|
1998
|
100 |
1 |
p. 77-83
7 p.
|
artikel
|
| 12 |
Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)
|
Roberts, Terry
|
|
1998
|
100 |
1 |
p. 10-20
11 p.
|
artikel
|
| 13 |
Occurrence of BCR-ABL rearrangement in a Philadelphia chromosome-negative patient with 5q and 13q deletions and myeloproliferative syndrome
|
Villegas, A
|
|
1998
|
100 |
1 |
p. 1-4
4 p.
|
artikel
|
| 14 |
Oncogenetic map of human genome
|
Verma, Ram S.
|
|
1998
|
100 |
1 |
p. 88-90
3 p.
|
artikel
|
| 15 |
10q deletions in metastatic cutaneous melanoma
|
Indsto, James O.
|
|
1998
|
100 |
1 |
p. 68-71
4 p.
|
artikel
|
| 16 |
Radiation therapy for breast cancer and clonal chromosome translocations: A fluorescence in situ hybridization study
|
Larramendy, Marcelo L.
|
|
1998
|
100 |
1 |
p. 57-62
6 p.
|
artikel
|
| 17 |
Sister chromatid exchange analysis of human cells carrying retroviral DNA
|
Koshikawa, Nobuko
|
|
1998
|
100 |
1 |
p. 72-76
5 p.
|
artikel
|
| 18 |
Sublocalization of the breakpoints of a t(5;16) in myelodysplasia
|
van Soest, Ronald A
|
|
1998
|
100 |
1 |
p. 5-9
5 p.
|
artikel
|
| 19 |
Trisomy 10 in acute myeloid leukemia: Report of a new case
|
Luño, Elisa
|
|
1998
|
100 |
1 |
p. 84-87
4 p.
|
artikel
|
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