| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Ataxin-7 expression analysis in controls and spinocerebellar ataxia type 7 patients
|
Einum, David D.
|
|
2001
|
3 |
2 |
p. 83-90
|
artikel
|
| 2 |
Ataxin-7 expression analysis in controls and spinocerebellar ataxia type 7 patients
|
Einum, David D.
|
|
2001
|
3 |
2 |
p. 83-90
|
artikel
|
| 3 |
Autism: evidence of association with adenosine deaminase genetic polymorphism
|
Bottini, Nunzio
|
|
2001
|
3 |
2 |
p. 111-113
|
artikel
|
| 4 |
Autism: evidence of association with adenosine deaminase genetic polymorphism
|
Bottini, Nunzio
|
|
2001
|
3 |
2 |
p. 111-113
|
artikel
|
| 5 |
Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathy
|
Bolino, Alessandra
|
|
2001
|
3 |
2 |
p. 107-109
|
artikel
|
| 6 |
Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathy
|
Bolino, Alessandra
|
|
2001
|
3 |
2 |
p. 107-109
|
artikel
|
| 7 |
Does (CUG)n repeat in DMPK mRNA ‘paint’ chromosome 19 to suppress distant genes to create the diverse phenotype of myotonic dystrophy?:
|
Junghans, R.P.
|
|
2001
|
3 |
2 |
p. 59-67
|
artikel
|
| 8 |
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonates
|
De Luca, Alessandro
|
|
2001
|
3 |
2 |
p. 79-82
|
artikel
|
| 9 |
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonates
|
De Luca, Alessandro
|
|
2001
|
3 |
2 |
p. 79-82
|
artikel
|
| 10 |
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia
|
Ashley-Koch, Allison
|
|
2001
|
3 |
2 |
p. 91-97
|
artikel
|
| 11 |
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia
|
Ashley-Koch, Allison
|
|
2001
|
3 |
2 |
p. 91-97
|
artikel
|
| 12 |
Hereditary demyelinating neuropathies: from gene to disease
|
Hanemann, C.O.
|
|
2001
|
3 |
2 |
p. 53-57
|
artikel
|
| 13 |
Hereditary demyelinating neuropathies: from gene to disease
|
Hanemann, C.O.
|
|
2001
|
3 |
2 |
p. 53-57
|
artikel
|
| 14 |
Mapping and sequencing rat dishevelled-1: a candidate gene for cerebral ischaemic insult in a rat model of stroke
|
De Lange, Robert P.J.
|
|
2001
|
3 |
2 |
p. 99-106
|
artikel
|
| 15 |
Mapping and sequencing rat dishevelled-1: a candidate gene for cerebral ischaemic insult in a rat model of stroke
|
De Lange, Robert P.J.
|
|
2001
|
3 |
2 |
p. 99-106
|
artikel
|
| 16 |
Nramp1 is expressed in neurons and is associated with behavioural and immune responses to stress
|
Evans, Carlton A.W.
|
|
2001
|
3 |
2 |
p. 69-78
|
artikel
|
| 17 |
Nramp1 is expressed in neurons and is associated with behavioural and immune responses to stress
|
Evans, Carlton A.W.
|
|
2001
|
3 |
2 |
p. 69-78
|
artikel
|
| 18 |
Online First publication
|
|
|
2001
|
3 |
2 |
p. 51
|
artikel
|
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