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Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood. [electronic resource] by
- Van Hove, J L
- Zhang, W
- Kahler, S G
- Roe, C R
- Chen, Y T
- Terada, N
- Chace, D H
- Iafolla, A K
- Ding, J H
- Millington, D S
Producer: 19930607
In:
American journal of human genetics vol. 52
Availability: No items available.
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17.
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The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients. [electronic resource] by
- Gibson, K M
- Christensen, E
- Jakobs, C
- Fowler, B
- Clarke, M A
- Hammersen, G
- Raab, K
- Kobori, J
- Moosa, A
- Vollmer, B
- Rossier, E
- Iafolla, A K
- Matern, D
- Brouwer, O F
- Finkelstein, J
- Aksu, F
- Weber, H P
- Bakkeren, J A
- Gabreels, F J
- Bluestone, D
- Barron, T F
- Beauvais, P
- Rabier, D
- Santos, C
- Lehnert, W
Producer: 19970425
In:
Pediatrics vol. 99
Availability: No items available.
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