nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A subtle t(3;8) results in plausible juxtaposition of MYC and BCL6 in a child with Burkitt lymphoma/leukemia and ataxia-telangiectasia
|
Sandlund, John T. |
|
2006 |
168 |
1 |
p. 69-72 4 p. |
artikel |
2 |
A t(17;20)(q21;q12) masking a variant t(15;17)(q22;q21) in a patient with acute promyelocytic leukemia
|
García-Casado, Zaida |
|
2006 |
168 |
1 |
p. 73-76 4 p. |
artikel |
3 |
Balanced t(11;15)(q23;q15) in a TP53 +/+ breast cancer patient from a Li–Fraumeni syndrome family
|
Sherif, Zaki A. |
|
2006 |
168 |
1 |
p. 50-58 9 p. |
artikel |
4 |
Breakpoint locations within chromosomes 1, 2, and 4 of patients with increased radiosensitivity
|
Schilling, Silke |
|
2006 |
168 |
1 |
p. 1-10 10 p. |
artikel |
5 |
Complex chromosomal rearrangements in patients with chronic myeloid leukemia
|
Babicka, Libuse |
|
2006 |
168 |
1 |
p. 22-29 8 p. |
artikel |
6 |
Detection of aberrations of ubiquitin-conjugating enzyme E2C gene (UBE2C) in advanced colon cancer with liver metastases by DNA microarray and two-color FISH
|
Takahashi, Yasuo |
|
2006 |
168 |
1 |
p. 30-35 6 p. |
artikel |
7 |
Editorial board
|
|
|
2006 |
168 |
1 |
p. CO2- 1 p. |
artikel |
8 |
Gross rearrangements in BRCA1 but not BRCA2 play a notable role in predisposition to breast and ovarian cancer in high-risk families of German origin
|
Preisler-Adams, Sabine |
|
2006 |
168 |
1 |
p. 44-49 6 p. |
artikel |
9 |
Molecular cytogenetic characterization of human papillomavirus16-transformed foreskin keratinocyte cell line 16-MT
|
McGhee, Eva M. |
|
2006 |
168 |
1 |
p. 36-43 8 p. |
artikel |
10 |
Molecular cytogenetic evaluation of 10 uveal melanoma cell lines
|
White, Jason S. |
|
2006 |
168 |
1 |
p. 11-21 11 p. |
artikel |
11 |
Neuroblastoma in an XYY male
|
Honma, Takahiro |
|
2006 |
168 |
1 |
p. 83-84 2 p. |
artikel |
12 |
Pediatric T-cell acute lymphoblastic leukemia with aberrations of both MLL loci
|
Quigley, Denise I. |
|
2006 |
168 |
1 |
p. 77-79 3 p. |
artikel |
13 |
Philadelphia chromosome of a constitutional der(22)t(Y;22)(q11.2;p11) with a variant t(1;9;22)(p36;q34;q11) in a case of chronic myelogenous leukemia
|
Buijs, Arjan |
|
2006 |
168 |
1 |
p. 80-82 3 p. |
artikel |
14 |
Table of contents
|
|
|
2006 |
168 |
1 |
p. A1-A2 nvt p. |
artikel |
15 |
Unique secondary chromosomal abnormalities are frequently found in the chronic phase of chronic myeloid leukemia in southern Vietnam
|
Xinh, Phan Thi |
|
2006 |
168 |
1 |
p. 59-68 10 p. |
artikel |