no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
Acknowledgement to Referees 2002-2004
|
|
|
2005 |
6 |
1 |
p. 57 |
article |
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 |
article |
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 |
article |
4 |
Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome
|
Asmus, Friedrich |
|
2004 |
6 |
1 |
p. 55-56 |
article |
5 |
Expanded FMR1 alleles are rare in idiopathic Parkinson’s disease
|
Tan, E. K. |
|
2004 |
6 |
1 |
p. 51-52 |
article |
6 |
Functional polymorphisms in the human β4 subunit of nicotinic acetylcholine receptors
|
Liang, Yong |
|
2004 |
6 |
1 |
p. 37-44 |
article |
7 |
Investigation of hormone receptor genes in migraine
|
Colson, Natalie J. |
|
2005 |
6 |
1 |
p. 17-23 |
article |
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 |
article |
9 |
NR2A and NR2B receptor gene variations modify age at onset in Huntington disease
|
Arning, Larissa |
|
2004 |
6 |
1 |
p. 25-28 |
article |
10 |
PLP1-related inherited dysmyelinating disorders: Pelizaeus-Merzbacher disease and spastic paraplegia type 2
|
Inoue, Ken |
|
2004 |
6 |
1 |
p. 1-16 |
article |
11 |
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer’s disease
|
Bagnoli, Silvia |
|
2004 |
6 |
1 |
p. 53-54 |
article |