| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abnormal dicentric chromosome with co-amplification of sequences from chromosomes 11 and 19
|
Smith, Arabella
|
|
2001
|
130 |
1 |
p. 29-32
4 p.
|
artikel
|
| 2 |
A new case of isolated del(12)(q15q22) in myelodysplastic syndrome
|
Fowler, Darren J.
|
|
2001
|
130 |
1 |
p. 89-91
3 p.
|
artikel
|
| 3 |
A new case of t(5;15)(p15;q11∼q13) in infant acute lymphoblastic leukemia
|
Silva, Maria Luiza M.
|
|
2001
|
130 |
1 |
p. 87-88
2 p.
|
artikel
|
| 4 |
A new complex variant t(4;15;17) in acute promyelocytic leukemia
|
Liu, Shihe
|
|
2001
|
130 |
1 |
p. 33-37
5 p.
|
artikel
|
| 5 |
B-cell acute lymphoblastic leukemia with tandem t(14;14)(q11;q32)
|
Berger, Roland
|
|
2001
|
130 |
1 |
p. 84-86
3 p.
|
artikel
|
| 6 |
CGH analysis of secondary genetic changes in Ewing tumors:
|
Brisset, Sophie
|
|
2001
|
130 |
1 |
p. 57-61
5 p.
|
artikel
|
| 7 |
Chromosome studies of murine T-cell lymphoid leukemia and derived cell lines
|
Fabris, Victoria
|
|
2001
|
130 |
1 |
p. 62-67
6 p.
|
artikel
|
| 8 |
Comparative genomic hybridization analysis identifies gains of 1p35∼p36 and chromosome 19 in osteosarcoma
|
Zielenska, Maria
|
|
2001
|
130 |
1 |
p. 14-21
8 p.
|
artikel
|
| 9 |
Comparative genomic hybridization and amplotyping by arbitrarily primed PCR in stage A B-CLL
|
Odero, Maria D
|
|
2001
|
130 |
1 |
p. 8-13
6 p.
|
artikel
|
| 10 |
Deletion of BCR region 3′ in chronic myelogenous leukemia
|
González, F.A
|
|
2001
|
130 |
1 |
p. 68-74
7 p.
|
artikel
|
| 11 |
Establishment and characterization of a new human myeloma cell line, KYδ-1, producing the δ/κ type immunoglobulin
|
Ueda, Chiyoko
|
|
2001
|
130 |
1 |
p. 42-50
9 p.
|
artikel
|
| 12 |
FISH characterization of t(8;12)(q12;p13) observed as the sole karyotypic anomaly in a myelodysplastic syndrome patient
|
Finelli, Palma
|
|
2001
|
130 |
1 |
p. 75-78
4 p.
|
artikel
|
| 13 |
Genetic alterations in hepatocellular carcinoma and intrahepatic cholangiocarcinoma
|
Koo, Sun Hoe
|
|
2001
|
130 |
1 |
p. 22-28
7 p.
|
artikel
|
| 14 |
Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics
|
Granzow, Martin
|
|
2001
|
130 |
1 |
p. 79-83
5 p.
|
artikel
|
| 15 |
Significant correlation between the breakpoints of rare clonal aberrations in benign solid tumors and the assignment of HMGIY retropseudogenes
|
Rogalla, Piere
|
|
2001
|
130 |
1 |
p. 51-56
6 p.
|
artikel
|
| 16 |
Translocation (14;19)(q32;q13) detected by spectral karyotyping and lack of BCL3 rearrangement in CD5-positive B-cell lymphoma associated with hemophagocytic syndrome
|
Yamamoto, Katsuya
|
|
2001
|
130 |
1 |
p. 38-41
4 p.
|
artikel
|
| 17 |
Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors
|
Sandberg, Avery A
|
|
2001
|
130 |
1 |
p. 1-7
7 p.
|
artikel
|
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