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A silent A to G mutation in exon 11 of the medium-chain acyl-CoA dehydrogenase (MCAD) gene. [electronic resource] by
- Andresen, B S
- Kølvraa, S
- Bross, P
- Bolund, L
- Curtis, D
- Eiberg, H
- Zhang, Z
- Kelly, D P
- Strauss, A W
- Gregersen, N
Producer: 19930702
In:
Human molecular genetics vol. 2
Availability: No items available.
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157.
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Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene. [electronic resource] by
- Tanaka, K
- Yokota, I
- Coates, P M
- Strauss, A W
- Kelly, D P
- Zhang, Z
- Gregersen, N
- Andresen, B S
- Matsubara, Y
- Curtis, D
Producer: 19930610
In:
Human mutation vol. 1
Availability: No items available.
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158.
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PPARalpha deficiency reduces insulin resistance and atherosclerosis in apoE-null mice. [electronic resource] by
- Tordjman, K
- Bernal-Mizrachi, C
- Zemany, L
- Weng, S
- Feng, C
- Zhang, F
- Leone, T C
- Coleman, T
- Kelly, D P
- Semenkovich, C F
Producer: 20010607
In:
The Journal of clinical investigation vol. 107
Availability: No items available.
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159.
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160.
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22q13 deletion syndrome. [electronic resource] by
- Phelan, M C
- Rogers, R C
- Saul, R A
- Stapleton, G A
- Sweet, K
- McDermid, H
- Shaw, S R
- Claytor, J
- Willis, J
- Kelly, D P
Producer: 20010712
In:
American journal of medical genetics vol. 101
Availability: No items available.
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