Results
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32381.
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32382.
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32383.
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32384.
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32385.
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32386.
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32387.
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32388.
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32389.
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32390.
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A new CYP2D6 allele with a nine base insertion in exon 9 in a Japanese population associated with poor metabolizer phenotype. [electronic resource] by
- Yokoi, T
- Kosaka, Y
- Chida, M
- Chiba, K
- Nakamura, H
- Ishizaki, T
- Kinoshita, M
- Sato, K
- Gonzalez, F J
- Kamataki, T
Producer: 19970314
In:
Pharmacogenetics vol. 6
Availability: No items available.
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32391.
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32392.
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32393.
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32394.
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32395.
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32396.
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32397.
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32398.
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Exclusion of familial dysautonomia from more than 60% of the genome. [electronic resource] by
- Blumenfeld, A
- Axelrod, F B
- Trofatter, J A
- Maayan, C
- Lucente, D E
- Slaugenhaupt, S A
- Liebert, C B
- Ozelius, L J
- Haines, J L
- Breakefield, X O
Producer: 19930219
In:
Journal of medical genetics vol. 30
Availability: No items available.
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32399.
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32400.
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