| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Analysis of exon dosage using MLPA in South African Parkinson's disease patients
|
Keyser, Rowena J.
|
|
2009
|
11 |
3 |
p. 305-312
|
artikel
|
| 2 |
Fine mapping of the chromosome 10q11-q21 linkage region in Alzheimer's disease cases and controls
|
Fallin, Margaret Daniele
|
|
2010
|
11 |
3 |
p. 335-348
|
artikel
|
| 3 |
Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19
|
Meilleur, K. G.
|
|
2009
|
11 |
3 |
p. 313-318
|
artikel
|
| 4 |
L239F founder mutation in GDAP1 is associated with a mild Charcot–Marie–Tooth type 4C4 (CMT4C4) phenotype
|
Kabzińska, Dagmara
|
|
2010
|
11 |
3 |
p. 357-366
|
artikel
|
| 5 |
Meta-analysis of association between variation in the PDE4D gene and ischemic cerebral infarction risk in Asian populations
|
Xu, Xiaowei
|
|
2010
|
11 |
3 |
p. 327-333
|
artikel
|
| 6 |
Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy
|
Yu, Dandan
|
|
2010
|
11 |
3 |
p. 349-356
|
artikel
|
| 7 |
Novel variants identified in methyl-CpG-binding domain genes in autistic individuals
|
Cukier, Holly N.
|
|
2009
|
11 |
3 |
p. 291-303
|
artikel
|
| 8 |
Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy
|
Kolb, Luis E.
|
|
2010
|
11 |
3 |
p. 319-325
|
artikel
|
| 9 |
Questionable association between a monoamine oxidase A promoter polymorphism and sudden infant death syndrome
|
Klintschar, Michael
|
|
2010
|
11 |
3 |
p. 367-368
|
artikel
|
| 10 |
RNA processing pathways in amyotrophic lateral sclerosis
|
Blitterswijk, Marka van
|
|
2010
|
11 |
3 |
p. 275-290
|
artikel
|
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