| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acute megakaryoblastic leukemia in an infant with a novel t(1;9)(p32;q34)
|
Hasegawa, Daiichiro
|
|
2000
|
122 |
1 |
p. 59-62
4 p.
|
artikel
|
| 2 |
Acute myeloid leukemia associated with hemophagocytic syndrome and t(4;7)(q21;q36)
|
Kumar, Manjusha
|
|
2000
|
122 |
1 |
p. 26-29
4 p.
|
artikel
|
| 3 |
Comparative genomic hybridization detects losses of chromosomes 22 and 16 as the most common recurrent genetic alterations in primary ependymomas
|
Zheng, Ping-pin
|
|
2000
|
122 |
1 |
p. 18-25
8 p.
|
artikel
|
| 4 |
Comparison of comparative genomic hybridization and interphase fluorescence in situ hybridization in ovarian carcinomas
|
Jacobsen, Anja
|
|
2000
|
122 |
1 |
p. 7-12
6 p.
|
artikel
|
| 5 |
Cytogenetic analysis in three cerebral subependymomas
|
Debiec-Rychter, Maria
|
|
2000
|
122 |
1 |
p. 63-64
2 p.
|
artikel
|
| 6 |
Deletion of Xq23 is a recurrent karyotypic abnormality in acute myeloid leukemia
|
Wong, K.F
|
|
2000
|
122 |
1 |
p. 33-36
4 p.
|
artikel
|
| 7 |
DNA replication error is frequent in ovarian granulosa cell tumors
|
Suzuki, Mitsuaki
|
|
2000
|
122 |
1 |
p. 55-58
4 p.
|
artikel
|
| 8 |
E-cadherin mutation-based genetic counseling and hereditary diffuse gastric carcinoma
|
Lynch, Henry T.
|
|
2000
|
122 |
1 |
p. 1-6
6 p.
|
artikel
|
| 9 |
hSNF5/INI1 gene mutations in lymphoid malignancy
|
Yuge, Masaaki
|
|
2000
|
122 |
1 |
p. 37-42
6 p.
|
artikel
|
| 10 |
Identification of chromosomes 3, 6, and 8 aberrations in uveal melanoma by microsatellite analysis in comparison to comparative genomic hybridization
|
Tschentscher, Frank
|
|
2000
|
122 |
1 |
p. 13-17
5 p.
|
artikel
|
| 11 |
Loss of heterozygosity at chromosomes 3, 6, 8, 11, 16, and 17 in ovarian cancer:
|
Launonen, Virpi
|
|
2000
|
122 |
1 |
p. 49-54
6 p.
|
artikel
|
| 12 |
Microdissection, DOP-PCR, and comparative genomic hybridization of paraffin-embedded familial prostate cancers
|
Verhagen, Paul C.M.S
|
|
2000
|
122 |
1 |
p. 43-48
6 p.
|
artikel
|
| 13 |
Recurrent chromosome aberrations in fibrous dysplasia of the bone
|
Dal Cin, Paola
|
|
2000
|
122 |
1 |
p. 30-32
3 p.
|
artikel
|
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