| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Alzheimer’s disease risk genes in wild-type adult zebrafish exhibit gender-specific expression changes during aging
|
Lee, Jinyoung
|
|
2016
|
17 |
3 |
p. 197-199
|
artikel
|
| 2 |
A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects
|
Beck, David B.
|
|
2016
|
17 |
3 |
p. 173-178
|
artikel
|
| 3 |
Genetic fitness and selection intensity in a population affected with high-incidence spinocerebellar ataxia type 1
|
Platonov, Fedor A.
|
|
2016
|
17 |
3 |
p. 179-185
|
artikel
|
| 4 |
Homozygous mutation in the APOA1BP is associated with a lethal infantile leukoencephalopathy
|
Spiegel, Ronen
|
|
2016
|
17 |
3 |
p. 187-190
|
artikel
|
| 5 |
microRNA profiling: increased expression of miR-147a and miR-518e in progressive supranuclear palsy (PSP)
|
Tatura, Roman
|
|
2016
|
17 |
3 |
p. 165-171
|
artikel
|
| 6 |
Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic features
|
Steinfeld, Hallie
|
|
2016
|
17 |
3 |
p. 159-164
|
artikel
|
| 7 |
Up-regulation of SNCA gene expression: implications to synucleinopathies
|
Tagliafierro, L.
|
|
2016
|
17 |
3 |
p. 145-157
|
artikel
|
| 8 |
Very mild features of dysequilibrium syndrome associated with a novel VLDLR missense mutation
|
Micalizzi, Alessia
|
|
2016
|
17 |
3 |
p. 191-195
|
artikel
|
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