nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Multicenter Investigation with D-FISH BCR/ABL1 Probes
|
Dewald, Gordon |
|
2000 |
116 |
2 |
p. 97-104 8 p. |
artikel |
2 |
Cellular Senescence of a Human Bladder Carcinoma Cell Line (JTC-32) Induced by a Normal Chromosome 11
|
Kugoh, Hiroyuki |
|
2000 |
116 |
2 |
p. 158-163 6 p. |
artikel |
3 |
Chronic Myeloid Leukemia with a Rare Variant Philadelphia Translocation
|
Guillaume, Benoı̂t |
|
2000 |
116 |
2 |
p. 166-169 4 p. |
artikel |
4 |
Complex Chromosome 9, 20, and 22 Rearrangements in Acute Lymphoblastic Leukemia with Duplication of BCR and ABL Sequences
|
Stevens-Kroef, M.J.P.L |
|
2000 |
116 |
2 |
p. 119-123 5 p. |
artikel |
5 |
DNA Copy Number Changes and Evaluation of MYC, IGF1R, and FES Amplification in Xenografts of Pancreatic Adenocarcinoma
|
Armengol, Gemma |
|
2000 |
116 |
2 |
p. 133-141 9 p. |
artikel |
6 |
Do Rosette, Heterochromatin, and/or Genomic Imprinting Influence Preferential Translocations in Human Neoplasia?
|
Verma, Ram S |
|
2000 |
116 |
2 |
p. 174-175 2 p. |
artikel |
7 |
Familial Acute Myeloid Leukemia with Monosomy 7
|
Kwong, Y.L |
|
2000 |
116 |
2 |
p. 170-173 4 p. |
artikel |
8 |
Fluorescence In Situ Hybridization Identifies Inversion 16 Masked by t(10;16)(q24;q22), t(7;16)(q21;q22), and t(2;16)(q37;q22) in Three Cases of AML-M4Eo
|
Reddy, K.S. |
|
2000 |
116 |
2 |
p. 148-152 5 p. |
artikel |
9 |
Full Cytogenetic Characterization of a New Neuroblastoma Cell Line with a Complex 17q Translocation
|
Panarello, Claudio |
|
2000 |
116 |
2 |
p. 124-132 9 p. |
artikel |
10 |
hRAD54 Gene and 1p High-Resolution Deletion-Mapping Analyses in Oligodendrogliomas
|
Bello, M.J |
|
2000 |
116 |
2 |
p. 142-147 6 p. |
artikel |
11 |
Multiplex Fluorescence In Situ Hybridization and Cross Species Color Banding of a Case of Chronic Myeloid Leukemia in Blastic Crisis with a Complex Philadelphia Translocation
|
Harrison, Christine J |
|
2000 |
116 |
2 |
p. 105-110 6 p. |
artikel |
12 |
Radiation-Associated Sarcomas are Characterized by Complex Karyotypes with Frequent Rearrangements of Chromosome Arm 3p
|
Mertens, Fredrik |
|
2000 |
116 |
2 |
p. 89-96 8 p. |
artikel |
13 |
Regional Fine Mapping of HMG17 to Chromosomal Band 1p35
|
Kazmierczak, Bernd |
|
2000 |
116 |
2 |
p. 164-165 2 p. |
artikel |
14 |
Translocation (8;13)(q24.2;q33) in a Malignant Rhabdoid Tumor of the Liver
|
Donner, Ludvik R |
|
2000 |
116 |
2 |
p. 153-157 5 p. |
artikel |
15 |
Trisomy 11 and a Complex t(11;11;22) in a Patient with Acute Myelomonocytic Leukemia (AML-M4) Following Myelodysplasia (MDS)
|
Bernasconi, P |
|
2000 |
116 |
2 |
p. 111-118 8 p. |
artikel |
16 |
Trisomy 15 in Hematological Disorders
|
Reddy, K.S |
|
2000 |
116 |
2 |
p. 176-177 2 p. |
artikel |