| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acknowledgement to Referees 2002-2004
|
|
|
2005
|
6 |
1 |
p. 57
|
artikel
|
| 2 |
A missense mutation in the coiled-coil motif of the HP1-interacting domain of ATR-X in a family with X-linked mental retardation
|
Wieland, Ilse
|
|
2004
|
6 |
1 |
p. 45-47
|
artikel
|
| 3 |
A novel out-of-frame mutation in the neurofilament light chain gene ( NEFL) does not result in Charcot-Marie-Tooth disease type 2E
|
Andrigo, Cinzia
|
|
2005
|
6 |
1 |
p. 49-50
|
artikel
|
| 4 |
Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome
|
Asmus, Friedrich
|
|
2004
|
6 |
1 |
p. 55-56
|
artikel
|
| 5 |
Expanded FMR1 alleles are rare in idiopathic Parkinson’s disease
|
Tan, E. K.
|
|
2004
|
6 |
1 |
p. 51-52
|
artikel
|
| 6 |
Functional polymorphisms in the human β4 subunit of nicotinic acetylcholine receptors
|
Liang, Yong
|
|
2004
|
6 |
1 |
p. 37-44
|
artikel
|
| 7 |
Investigation of hormone receptor genes in migraine
|
Colson, Natalie J.
|
|
2005
|
6 |
1 |
p. 17-23
|
artikel
|
| 8 |
MLPA analysis for the detection of deletions, duplications and complex rearrangements in the dystrophin gene: potential and pitfalls
|
Janssen, B.
|
|
2005
|
6 |
1 |
p. 29-35
|
artikel
|
| 9 |
NR2A and NR2B receptor gene variations modify age at onset in Huntington disease
|
Arning, Larissa
|
|
2004
|
6 |
1 |
p. 25-28
|
artikel
|
| 10 |
PLP1-related inherited dysmyelinating disorders: Pelizaeus-Merzbacher disease and spastic paraplegia type 2
|
Inoue, Ken
|
|
2004
|
6 |
1 |
p. 1-16
|
artikel
|
| 11 |
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer’s disease
|
Bagnoli, Silvia
|
|
2004
|
6 |
1 |
p. 53-54
|
artikel
|
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