| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel BAP1 mutation is associated with melanocytic neoplasms and thyroid cancer
|
McDonnell, Kevin J.
|
|
2016
|
209 |
3 |
p. 75-81
7 p.
|
artikel
|
| 2 |
A t(11;14)(p13;q11.2) in myelofibrosis following polycythemia vera
|
Jeong, Ji Hun
|
|
2016
|
209 |
3 |
p. 112-116
5 p.
|
artikel
|
| 3 |
Cover_spine
|
|
|
2016
|
209 |
3 |
p. CO1-
1 p.
|
artikel
|
| 4 |
Disruption of the APC gene by t(5;7) translocation in a Turcot family
|
Sahnane, Nora
|
|
2016
|
209 |
3 |
p. 107-111
5 p.
|
artikel
|
| 5 |
Distinct set of chromosomal aberrations in childhood hepatocellular carcinoma is correlated to hepatitis B virus infection
|
Tan, Lu
|
|
2016
|
209 |
3 |
p. 87-96
10 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2016
|
209 |
3 |
p. CO2-
1 p.
|
artikel
|
| 7 |
Optimal strategy for obtaining routine chromosome analysis by using negative fractions of CD138 enriched plasma cells
|
Ortega, Veronica
|
|
2016
|
209 |
3 |
p. 82-86
5 p.
|
artikel
|
| 8 |
Overview of recurrent chromosomal losses in retinoblastoma detected by low coverage next generation sequencing
|
García-Chequer, A.J.
|
|
2016
|
209 |
3 |
p. 57-69
13 p.
|
artikel
|
| 9 |
Rare germline variant (rs78378222) in the TP53 3' UTR: Evidence for a new mechanism of cancer predisposition in Li-Fraumeni syndrome
|
Macedo, Gabriel S.
|
|
2016
|
209 |
3 |
p. 97-106
10 p.
|
artikel
|
| 10 |
Table of Contents
|
|
|
2016
|
209 |
3 |
p. A1-
1 p.
|
artikel
|
| 11 |
The peculiar 11q-gain/loss aberration reported in a subset of MYC-negative high-grade B-cell lymphomas can also occur in a MYC-rearranged lymphoma
|
Havelange, Violaine
|
|
2016
|
209 |
3 |
p. 117-118
2 p.
|
artikel
|
| 12 |
The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers
|
Laitman, Yael
|
|
2016
|
209 |
3 |
p. 70-74
5 p.
|
artikel
|
Tijdschrift beschrijving