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Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency. [electronic resource] by
- Van Kuilenburg, A B
- Vreken, P
- Abeling, N G
- Bakker, H D
- Meinsma, R
- Van Lenthe, H
- De Abreu, R A
- Smeitink, J A
- Kayserili, H
- Apak, M Y
- Christensen, E
- Holopainen, I
- Pulkki, K
- Riva, D
- Botteon, G
- Holme, E
- Tulinius, M
- Kleijer, W J
- Beemer, F A
- Duran, M
- Niezen-Koning, K E
- Smit, G P
- Jakobs, C
- Smit, L M
- Van Gennip, A H
Producer: 19990316
In:
Human genetics vol. 104
Availability: No items available.
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Nomenclature for human DPYD alleles. [electronic resource] by
- McLeod, H L
- Collie-Duguid, E S
- Vreken, P
- Johnson, M R
- Wei, X
- Sapone, A
- Diasio, R B
- Fernandez-Salguero, P
- van Kuilenberg, A B
- van Gennip, A H
- Gonzalez, F J
Producer: 19990329
In:
Pharmacogenetics vol. 8
Availability: No items available.
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Partial epilepsy in a girl with a symptom-free sister: first two Finnish patients with dihydropyrimidine dehydrogenase deficiency. [electronic resource] by
- Holopainen, I
- Pulkki, K
- Heinonen, O J
- Näntö-Salonen, K
- Haataja, L
- Greter, J
- Holme, E
- van Kuilenburg, A B
- Vreken, P
- van Gennip, A H
Producer: 19971106
In:
Journal of inherited metabolic disease vol. 20
Availability: No items available.
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