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Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia. [electronic resource] by
- Slaugenhaupt, S A
- Blumenfeld, A
- Gill, S P
- Leyne, M
- Mull, J
- Cuajungco, M P
- Liebert, C B
- Chadwick, B
- Idelson, M
- Reznik, L
- Robbins, C
- Makalowska, I
- Brownstein, M
- Krappmann, D
- Scheidereit, C
- Maayan, C
- Axelrod, F B
- Gusella, J F
Producer: 20010405
In:
American journal of human genetics vol. 68
Availability: No items available.
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Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31. [electronic resource] by
- Blumenfeld, A
- Slaugenhaupt, S A
- Liebert, C B
- Temper, V
- Maayan, C
- Gill, S
- Lucente, D E
- Idelson, M
- MacCormack, K
- Monahan, M A
- Mull, J
- Leyne, M
- Mendillo, M
- Schiripo, T
- Mishori, E
- Breakefield, X
- Axelrod, F B
- Gusella, J F
Producer: 20000405
In:
American journal of human genetics vol. 64
Availability: No items available.
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