| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acute lymphoblastic leukemia and lymphoma in the context of constitutional mismatch repair deficiency syndrome
|
Ripperger, Tim
|
|
2016
|
59 |
3 |
p. 133-142
10 p.
|
artikel
|
| 2 |
Acute lymphoblastic leukemia in the context of RASopathies
|
Cavé, Hélène
|
|
2016
|
59 |
3 |
p. 173-178
6 p.
|
artikel
|
| 3 |
Clinical course and therapeutic implications for lymphoid malignancies in Nijmegen breakage syndrome
|
Pastorczak, Agata
|
|
2016
|
59 |
3 |
p. 126-132
7 p.
|
artikel
|
| 4 |
Constitutional abnormalities of chromosome 21 predispose to iAMP21-acute lymphoblastic leukaemia
|
Harrison, Christine J.
|
|
2016
|
59 |
3 |
p. 162-165
4 p.
|
artikel
|
| 5 |
Fanconi anemia with biallelic FANCD1/BRCA2 mutations – Case report of a family with three affected children
|
Svojgr, Karel
|
|
2016
|
59 |
3 |
p. 152-157
6 p.
|
artikel
|
| 6 |
GEMMs addressing Pax5 loss-of-function in childhood pB-ALL
|
Auer, Franziska
|
|
2016
|
59 |
3 |
p. 166-172
7 p.
|
artikel
|
| 7 |
Genetic predisposition to acute lymphoblastic leukemia: Overview on behalf of the I-BFM ALL Host Genetic Variation Working Group
|
Kratz, Christian Peter
|
|
2016
|
59 |
3 |
p. 111-115
5 p.
|
artikel
|
| 8 |
Preexisting conditions in pediatric ALL patients: Spectrum, frequency and clinical impact
|
Schütte, P.
|
|
2016
|
59 |
3 |
p. 143-151
9 p.
|
artikel
|
| 9 |
Recognition of genetic predisposition in pediatric cancer patients: An easy-to-use selection tool
|
Jongmans, Marjolijn C.J.
|
|
2016
|
59 |
3 |
p. 116-125
10 p.
|
artikel
|
| 10 |
The acute lymphoblastic leukemia of Down Syndrome – Genetics and pathogenesis
|
Izraeli, Shai
|
|
2016
|
59 |
3 |
p. 158-161
4 p.
|
artikel
|
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