nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A leukemic double-hit follicular lymphoma associated with a complex variant translocation, t(8;14;18)(q24;q32;q21), involving BCL2, MYC, and IGH
|
Minakata, Daisuke |
|
2018 |
220 |
C |
p. 44-48 |
artikel |
2 |
APRIL gene expression in a cohort of Egyptian acute myeloid leukemia patients: Clinical and prognostic significance
|
Hammam, Amira Ahmed |
|
2018 |
220 |
C |
p. 24-31 |
artikel |
3 |
Assessment of a FBXW8 frameshift mutation, c.1312_1313delGT, in breast cancer patients and controls from Central Europe
|
Wang, Jing |
|
2018 |
220 |
C |
p. 38-43 |
artikel |
4 |
Circulating long non-coding RNA MALAT1 expression as molecular biomarker in Egyptian patients with breast cancer
|
Zidan, Haidy E. |
|
2018 |
220 |
C |
p. 32-37 |
artikel |
5 |
Comprehensive BRCA mutation analysis in the Greek population. Experience from a single clinical diagnostic center
|
Apessos, Angela |
|
2018 |
220 |
C |
p. 1-12 |
artikel |
6 |
Decoding colorectal cancer epigenomics
|
El Bairi, Khalid |
|
2018 |
220 |
C |
p. 49-76 |
artikel |
7 |
Discussion on reply to Foley et al., ‘Acute myeloid leukemia with t(14;21) involving RUNX1 and SYNE2: A novel favorable-risk translocation?’
|
Mannis, Gabriel N. |
|
2018 |
220 |
C |
p. 77-78 |
artikel |
8 |
Editorial Board
|
|
|
2018 |
220 |
C |
p. ii |
artikel |
9 |
Genetic analysis and clinical description of Greek patients with Peutz-Jeghers syndrome: Creation of a National Registry
|
Fostira, Florentia |
|
2018 |
220 |
C |
p. 19-23 |
artikel |
10 |
Myeloid neoplasm with eosinophilia associated with isolated extramedullary FIP1L1/PDGFRA rearrangement
|
Hilal, Talal |
|
2018 |
220 |
C |
p. 13-18 |
artikel |
11 |
Reply to Foley et al., “Acute myeloid leukemia with t(14;21) involving RUNX1 and SYNE2: A novel favorable-risk translocation?”
|
Sorigue, Marc |
|
2018 |
220 |
C |
p. 77 |
artikel |