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Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B. [electronic resource] by
- Kulkens, T
- Bolhuis, P A
- Wolterman, R A
- Kemp, S
- te Nijenhuis, S
- Valentijn, L J
- Hensels, G W
- Jennekens, F G
- de Visser, M
- Hoogendijk, J E
Producer: 19931209
In:
Nature genetics vol. 5
Availability: No items available.
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Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspects. [electronic resource] by
- Jöbsis, G J
- Louwerse, E S
- de Visser, M
- Wolterman, R A
- Bolhuis, P A
- Busch, H F
- Brüggenwirth, H T
- Baas, F
- Wiersinga, W M
- Koelman, J H
Producer: 19951124
In:
Journal of the neurological sciences vol. 129 Suppl
Availability: No items available.
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13.
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Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations. [electronic resource] by
- Kemp, S
- Ligtenberg, M J
- van Geel, B M
- Barth, P G
- Wolterman, R A
- Schoute, F
- Sarde, C O
- Mandel, J L
- van Oost, B A
- Bolhuis, P A
Producer: 19940901
In:
Biochemical and biophysical research communications vol. 202
Availability: No items available.
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