| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Allelic imbalance and fine mapping of the 17p13.3 subregion in sporadic breast carcinomas
|
Hoff, Céline
|
|
2001
|
129 |
2 |
p. 145-149
5 p.
|
artikel
|
| 2 |
Aneurysmal bone cyst with chromosomal changes involving 7q and 16p
|
Baruffi, M.R
|
|
2001
|
129 |
2 |
p. 177-180
4 p.
|
artikel
|
| 3 |
An hsr on chromosome 7 was shown to be an insertion of four copies of the 11q23 MLL gene region in an HIV-related lymphoma
|
Reddy, Kavita S
|
|
2001
|
129 |
2 |
p. 107-111
5 p.
|
artikel
|
| 4 |
A unique AML1 (CBF2A) rearrangement, t(1;21)(p32;q22), observed in a patient with acute myelomonocytic leukemia
|
Cherry, Athena M
|
|
2001
|
129 |
2 |
p. 155-160
6 p.
|
artikel
|
| 5 |
Characteristics of chromosome instability in the human lymphoblast cell line WTK1
|
Schwartz, Jeffrey L
|
|
2001
|
129 |
2 |
p. 124-130
7 p.
|
artikel
|
| 6 |
Chronic T-cell lymphoproliferative disease expressing natural killer cell receptors
|
Kwong, Y.L
|
|
2001
|
129 |
2 |
p. 168-172
5 p.
|
artikel
|
| 7 |
Clonal chromosome rearrangements in hairy cell leukemia
|
Sambani, Constantina
|
|
2001
|
129 |
2 |
p. 138-144
7 p.
|
artikel
|
| 8 |
Detection of a novel t(6;15)(q21;q21) in a pediatric Wilms tumor
|
Fernandez, Conrad V
|
|
2001
|
129 |
2 |
p. 165-167
3 p.
|
artikel
|
| 9 |
Erratum
|
|
|
2001
|
129 |
2 |
p. 183-
1 p.
|
artikel
|
| 10 |
Exclusion of large deletions and other rearrangements in BRCA1 and BRCA2 in Finnish breast and ovarian cancer families
|
Lahti-Domenici, Jaana
|
|
2001
|
129 |
2 |
p. 120-123
4 p.
|
artikel
|
| 11 |
Identification of a 1.2 Kb cDNA fragment from a region on 9p21 commonly deleted in multiple tumor types
|
Gursky, Susan
|
|
2001
|
129 |
2 |
p. 93-101
9 p.
|
artikel
|
| 12 |
Large deletion of part of the HMGIC locus accompanying a t(3;12)(q27∼q28;q14∼q15) in a lipoma
|
Lemke, Inga
|
|
2001
|
129 |
2 |
p. 161-164
4 p.
|
artikel
|
| 13 |
Localization of the chromosome 22 breakpoints in two cases of acute megakaryoblastic leukemia with t(1;22)(p13;q13)
|
Dickstein, Jerome I
|
|
2001
|
129 |
2 |
p. 150-154
5 p.
|
artikel
|
| 14 |
Molecular characterization of the breakpoint region associated with a constitutional t(2;15)(q34;q26) in a patient with multiple myeloma
|
Kitamura, Eiko
|
|
2001
|
129 |
2 |
p. 112-119
8 p.
|
artikel
|
| 15 |
No DNA sequence copy number changes in essential thrombocythemia
|
Larramendy, Marcelo L
|
|
2001
|
129 |
2 |
p. 181-182
2 p.
|
artikel
|
| 16 |
Routine fluorescence in situ hybridization with the MLL probe does not reliably detect two separate signals on one chromosome 11 in patients with trisomy 11
|
Smith, A
|
|
2001
|
129 |
2 |
p. 173-176
4 p.
|
artikel
|
| 17 |
Supernumerary ring chromosomes in dermatofibrosarcoma protuberans may contain sequences from 8q11.2∼qter and 17q21∼qter
|
Nishio, Jun
|
|
2001
|
129 |
2 |
p. 102-106
5 p.
|
artikel
|
| 18 |
Suppression of tumorigenicity in human ovarian carcinoma cell line SKOV-3 by microcell-mediated transfer of chromosome 11
|
Cao, Qiag
|
|
2001
|
129 |
2 |
p. 131-137
7 p.
|
artikel
|
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