| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family
|
Baysal, Bora E.
|
|
2002
|
4 |
1 |
p. 43-53
|
artikel
|
| 2 |
A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family
|
Baysal, Bora E.
|
|
2002
|
4 |
1 |
p. 43-53
|
artikel
|
| 3 |
A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze family
|
Delague, Valérie
|
|
2002
|
4 |
1 |
p. 23-27
|
artikel
|
| 4 |
A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze family
|
Delague, Valérie
|
|
2002
|
4 |
1 |
p. 23-27
|
artikel
|
| 5 |
A typical migraine susceptibility region localizes to chromosome 1q31
|
Lea, Rod A.
|
|
2002
|
4 |
1 |
p. 17-22
|
artikel
|
| 6 |
A typical migraine susceptibility region localizes to chromosome 1q31
|
Lea, Rod A.
|
|
2002
|
4 |
1 |
p. 17-22
|
artikel
|
| 7 |
Expression of the survival of motor neuron (SMN) gene in primary neurons and increase in SMN levels by activation of the N-methyl-D-aspartate glutamate receptor
|
Andreassi, Catia
|
|
2002
|
4 |
1 |
p. 29-36
|
artikel
|
| 8 |
Expression of the survival of motor neuron (SMN) gene in primary neurons and increase in SMN levels by activation of the N-methyl-D-aspartate glutamate receptor
|
Andreassi, Catia
|
|
2002
|
4 |
1 |
p. 29-36
|
artikel
|
| 9 |
Identification of polymorphisms within the bovine prion protein gene (Prnp) by DNA sequencing and genotyping by MALDI-TOF-MS
|
Humeny, Andreas
|
|
2002
|
4 |
1 |
p. 59-60
|
artikel
|
| 10 |
Molecular cell biology of Charcot-Marie-Tooth disease
|
Berger, Philipp
|
|
2002
|
4 |
1 |
p. 1-15
|
artikel
|
| 11 |
Molecular cell biology of Charcot-Marie-Tooth disease
|
Berger, Philipp
|
|
2002
|
4 |
1 |
p. 1-15
|
artikel
|
| 12 |
Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathies
|
Venken, Koen
|
|
2001
|
4 |
1 |
p. 37-41
|
artikel
|
| 13 |
Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathies
|
Venken, Koen
|
|
2001
|
4 |
1 |
p. 37-41
|
artikel
|
| 14 |
Sequence analysis of two nuclear encoded subunits (10 and 51 kDa) of mitochondrial complex I in Parkinson disease
|
Grasbon-Frodl, Eva M.
|
|
2002
|
4 |
1 |
p. 55-57
|
artikel
|
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