nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A case of follicular small cleaved cell lymphoma with t(14;18) and t(8;11)
|
Bal, S. |
|
1990 |
48 |
2 |
p. 199-201 3 p. |
artikel |
2 |
American Burkitt lymphoma stage II with 47,XY,+20,t(8;14)(q24;q32)
|
Xiao, Han |
|
1990 |
48 |
2 |
p. 275-277 3 p. |
artikel |
3 |
Apparent lack of telomere sequences on double minute chromosomes
|
Lin, C.C. |
|
1990 |
48 |
2 |
p. 271-274 4 p. |
artikel |
4 |
Chronic myeloid leukemia with unusual variant Ph translocation (22;22)(q11;q13)
|
Laï, J.L. |
|
1990 |
48 |
2 |
p. 209-216 8 p. |
artikel |
5 |
c-myb gene analysis in T-cell malignancies with del(6q)
|
Okada, Michiko |
|
1990 |
48 |
2 |
p. 229-236 8 p. |
artikel |
6 |
Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas
|
Nilbert, Mef |
|
1990 |
48 |
2 |
p. 217-223 7 p. |
artikel |
7 |
Cytogenetic study of solid ovarian tumors
|
Roberts, Cynthia G. |
|
1990 |
48 |
2 |
p. 243-253 11 p. |
artikel |
8 |
Deletion of part of the short arm of chromosome 17 in a congenital fibrosarcoma
|
Gorman, Patricia A. |
|
1990 |
48 |
2 |
p. 193-198 6 p. |
artikel |
9 |
Detection by electron microscopy of a small subband 13q14.11 deletion in an hereditary retinoblastoma
|
Lemieux, Nicole |
|
1990 |
48 |
2 |
p. 265-269 5 p. |
artikel |
10 |
Human malignant melanoma significance of chromosomal abnormalities
|
Grammatico, P. |
|
1990 |
48 |
2 |
p. 237-242 6 p. |
artikel |
11 |
In vitro cytogenetic effects of recombinant human hematopoietic growth factors on cells derived from myelodysplastic syndromes
|
Ohyashiki, Kazuma |
|
1990 |
48 |
2 |
p. 169-178 10 p. |
artikel |
12 |
Involvement of both chromosomes 5 in a patient with leukemia secondary to myelodysplastic syndrome
|
Berkowicz, M. |
|
1990 |
48 |
2 |
p. 279-280 2 p. |
artikel |
13 |
Isochromosome (8q) in four patients with adenocarcinoma of the lung
|
Miura, Ikuo |
|
1990 |
48 |
2 |
p. 203-207 5 p. |
artikel |
14 |
New example of 6p involvement in lipoma
|
|
|
1990 |
48 |
2 |
p. 281-283 3 p. |
artikel |
15 |
No evidence of trisomy 12 or t(11;14) by molecular genetic techniques in chronic lymphocytic leukemia cells with a normal karyotype
|
Einhorn, Stefan |
|
1990 |
48 |
2 |
p. 183-192 10 p. |
artikel |
16 |
Parathyroid adenoma with t(1;5)(p22;q32) as the sole clonal chromosome abnormality
|
Örndal, Charlotte |
|
1990 |
48 |
2 |
p. 225-228 4 p. |
artikel |
17 |
Pathogenesis of adult testicular germ cell tumors
|
de Jong, Bauke |
|
1990 |
48 |
2 |
p. 143-167 25 p. |
artikel |
18 |
“Pseudodicentric isochromosome(22) in meningiomas”
|
|
|
1990 |
48 |
2 |
p. 284- 1 p. |
artikel |
19 |
t(2;14)(q23;q32.3) as the sole abnormality in a patient with acute nonlymphocytic leukemia (FAB-M4)
|
Columbano-Green, Letizia M. |
|
1990 |
48 |
2 |
p. 255-257 3 p. |
artikel |
20 |
Trisomy 13 and myelodysplastic syndrome
|
Beverstock, Geoffrey C. |
|
1990 |
48 |
2 |
p. 179-182 4 p. |
artikel |
21 |
Trisomy 21 in transient myeloproliferative disorder
|
Faed, M.J.W. |
|
1990 |
48 |
2 |
p. 259-264 6 p. |
artikel |