nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An evaluation of SOX2 and hTERC gene amplifications as screening markers in oral and oropharyngeal squamous cell carcinomas
|
Kokalj Vokač, Nadja |
|
2014 |
7 |
1 |
|
artikel |
2 |
Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first, second or third trimester: QF-PCR, karyotyping and/or genome wide SNP array analysis
|
Kooper, Angelique JA |
|
2014 |
7 |
1 |
|
artikel |
3 |
Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability
|
Xu, Fang |
|
2014 |
7 |
1 |
|
artikel |
4 |
De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis
|
Schwaibold, Eva Maria Christina |
|
2014 |
7 |
1 |
|
artikel |
5 |
Differences and homologies of chromosomal alterations within and between breast cancer cell lines: a clustering analysis
|
Rondón-Lagos, Milena |
|
2014 |
7 |
1 |
|
artikel |
6 |
Homozygous deletion of TNFRSF4, TP73, PPAP2B and DPYD at 1p and PDCD5 at 19q identified by multiplex ligation-dependent probe amplification (MLPA) analysis in pediatric anaplastic glioma with questionable oligodendroglial component
|
Torres-Martín, Miguel |
|
2014 |
7 |
1 |
|
artikel |
7 |
Identification of prognostic relevant chromosomal abnormalities in chronic lymphocytic leukemia using microarray-based genomic profiling
|
Stevens-Kroef, Marian JPL |
|
2014 |
7 |
1 |
|
artikel |
8 |
In memoriam of Anna D Polityko (17.12.1959 — 20.04.2013)
|
Iourov, Ivan |
|
2014 |
7 |
1 |
|
artikel |
9 |
MECP2 duplication phenotype in symptomatic females: report of three further cases
|
Novara, Francesca |
|
2014 |
7 |
1 |
|
artikel |
10 |
Reviewer acknowledgement 2014
|
Liehr, Thomas |
|
2014 |
7 |
1 |
|
artikel |