| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations
|
Stouffs, Katrien
|
|
2018
|
61 |
12 |
p. 733-737
|
artikel
|
| 2 |
Editorial Board
|
|
|
2018
|
61 |
12 |
p. ii
|
artikel
|
| 3 |
Further refinement of COL4A1 and COL4A2 related cortical malformations
|
Cavallin, Mara
|
|
2018
|
61 |
12 |
p. 765-772
|
artikel
|
| 4 |
Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis
|
Vandervore, Laura V.
|
|
2018
|
61 |
12 |
p. 783-789
|
artikel
|
| 5 |
Mutations in TBR1 gene leads to cortical malformations and intellectual disability
|
Vegas, Nancy
|
|
2018
|
61 |
12 |
p. 759-764
|
artikel
|
| 6 |
Neuro-MIG: A European network on brain malformations
|
Mancini, Grazia M.S.
|
|
2018
|
61 |
12 |
p. 741-743
|
artikel
|
| 7 |
Polymicrogyria in association with hypoglycemia points to mutation in the mTOR pathway
|
Stutterd, Chloe
|
|
2018
|
61 |
12 |
p. 738-740
|
artikel
|
| 8 |
Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome
|
Deloison, B.
|
|
2018
|
61 |
12 |
p. 773-782
|
artikel
|
| 9 |
Recurrent RTTN mutation leading to severe microcephaly, polymicrogyria and growth restriction
|
Cavallin, Mara
|
|
2018
|
61 |
12 |
p. 755-758
|
artikel
|
| 10 |
TLE1, a key player in neurogenesis, a new candidate gene for autosomal recessive postnatal microcephaly
|
Cavallin, Mara
|
|
2018
|
61 |
12 |
p. 729-732
|
artikel
|
| 11 |
Tubulin genes and malformations of cortical development
|
Romaniello, Romina
|
|
2018
|
61 |
12 |
p. 744-754
|
artikel
|
Tijdschrift beschrijving