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Tijdschrift beschrijving
Alle jaargangen van het bijbehorende tijdschrift
Alle afleveringen van het bijbehorende jaargang
Alle artikelen van de bijbehorende aflevering
6 gevonden resultaten
| nr | titel | auteur | tijdschrift | jaar | jaarg. | afl. | pagina('s) | type |
| 1 | ADCY5-related dyskinesia presenting as familial myoclonus-dystonia |
Douglas, Andrew G. L. |
2017 |
18 | 2 |
p. 111-117 |
artikel |
|
| 2 | Analysis of gene expression in the nervous system identifies key genes and novel candidates for health and disease |
Carpanini, Sarah M |
2017 |
18 | 2 |
p. 81-95 |
artikel |
|
| 3 | Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect |
Shahrour, Maher Awni |
2017 |
18 | 2 |
p. 119 |
artikel |
|
| 4 | Identification and functional characterization of a novel MTFMT mutation associated with selective vulnerability of the visual pathway and a mild neurological phenotype |
La Piana, Roberta |
2017 |
18 | 2 |
p. 97-103 |
artikel |
|
| 5 | Recurrent KIF2A mutations are responsible for classic lissencephaly |
Cavallin, Mara |
2016 |
18 | 2 |
p. 73-79 |
artikel |
|
| 6 | TFG associated hereditary spastic paraplegia: an addition to the phenotypic spectrum |
Tariq, Huma |
2017 |
18 | 2 |
p. 105-109 |
artikel |
6 gevonden resultaten