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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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29.
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Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency. [electronic resource] by
- Andresen, B S
- Dobrowolski, S F
- O'Reilly, L
- Muenzer, J
- McCandless, S E
- Frazier, D M
- Udvari, S
- Bross, P
- Knudsen, I
- Banas, R
- Chace, D H
- Engel, P
- Naylor, E W
- Gregersen, N
Producer: 20010705
In:
American journal of human genetics vol. 68
Availability: No items available.
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