| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4 ) localizes to a 500-kb interval on chromosome 9q34
|
Blair, I. P.
|
|
2000
|
3 |
1 |
p. 1-6
|
artikel
|
| 2 |
Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32 ), peripheral myelin protein 22 (PMP22 ), and peripheral myelin protein zero (MPZ )
|
Ekici, A. B.
|
|
2000
|
3 |
1 |
p. 49-50
|
artikel
|
| 3 |
CLN -encoded proteins do not interact with each other
|
Zhong, N. A.
|
|
2000
|
3 |
1 |
p. 41-44
|
artikel
|
| 4 |
Developmental profile of Sry transcripts in mouse brain
|
Mayer, A.
|
|
2000
|
3 |
1 |
p. 25-30
|
artikel
|
| 5 |
Evidence for allelic association of the dopamine β-hydroxylase gene (DBH) with susceptibility to typical migraine
|
Lea, R. A.
|
|
2000
|
3 |
1 |
p. 35-40
|
artikel
|
| 6 |
Mutation analysis of the hCHK2 gene in primary human malignant gliomas
|
Louis, D. N.
|
|
2000
|
3 |
1 |
p. 45-46
|
artikel
|
| 7 |
Sequence analysis of the MTCYB gene in Parkinson disease
|
von Eitzen, U.
|
|
2000
|
3 |
1 |
p. 47-48
|
artikel
|
| 8 |
Supporting evidence of a gene for partial epilepsy on 10q
|
Mautner, V.-F.
|
|
2000
|
3 |
1 |
p. 31-34
|
artikel
|
| 9 |
The parental origin of new mutations in neurofibromatosis 2
|
Kluwe, L.
|
|
2000
|
3 |
1 |
p. 17-24
|
artikel
|
| 10 |
The survival motor neuron (SMN) protein: effect of exon loss and mutation on protein localization
|
Le, T. T.
|
|
2000
|
3 |
1 |
p. 7-16
|
artikel
|
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