| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Chromosome 7 heteromorphism
|
Mark, Hon Fong L
|
|
2000
|
123 |
2 |
p. 144-
1 p.
|
artikel
|
| 2 |
Common chromosome aberrations in the proximal type of epithelioid sarcoma
|
Debiec-Rychter, Maria
|
|
2000
|
123 |
2 |
p. 133-136
4 p.
|
artikel
|
| 3 |
Detection of t(14;18)(q32;q21) in hyperdiploid cells by fluorescence in situ hybridization in a patient with Hodgkin disease
|
Miura, Ikuo
|
|
2000
|
123 |
2 |
p. 97-101
5 p.
|
artikel
|
| 4 |
Importance of using comparative genomic hybridization to improve detection of chromosomal changes in childhood acute lymphoblastic leukemia
|
Jaroπová, Marie
|
|
2000
|
123 |
2 |
p. 114-122
9 p.
|
artikel
|
| 5 |
Index
|
|
|
2000
|
123 |
2 |
p. 145-150
6 p.
|
artikel
|
| 6 |
Index
|
|
|
2000
|
123 |
2 |
p. 151-165
15 p.
|
artikel
|
| 7 |
Loss of heterozygosity at 1p, 8p, 10p, 13q, and 17p in advanced urothelial cancer and lack of relation to chemotherapy response and outcome
|
Sengeløv, Lisa
|
|
2000
|
123 |
2 |
p. 109-113
5 p.
|
artikel
|
| 8 |
Novel findings in gene expression detected in human osteosarcoma by cDNA microarray
|
Wolf, Maija
|
|
2000
|
123 |
2 |
p. 128-132
5 p.
|
artikel
|
| 9 |
Standardization criteria for the detection of BCR/ABL fusion in interphase nuclei of chronic myelogenous leukemia patients by fluorescence in situ hybridization
|
Cohen, Ninette
|
|
2000
|
123 |
2 |
p. 102-108
7 p.
|
artikel
|
| 10 |
Static cytometry identifies hyperdiploid childhood ALL
|
van den Berghe, Janette A
|
|
2000
|
123 |
2 |
p. 123-127
5 p.
|
artikel
|
| 11 |
Trisomy 1q, 2, and 20 in a case of hepatoblastoma
|
Yeh, Y.Albert
|
|
2000
|
123 |
2 |
p. 140-143
4 p.
|
artikel
|
| 12 |
Typical CBFβ/MYH11 fusion due to insertion of the 3′-MYH11 gene into 16q22 in acute monocytic leukemia with normal chromosomes 16 and trisomies 8 and 22
|
Aventı́n, Anna
|
|
2000
|
123 |
2 |
p. 137-139
3 p.
|
artikel
|
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