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Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study. [electronic resource] by
- He, Y
- Jones, K J
- Vignier, N
- Morgan, G
- Chevallay, M
- Barois, A
- Estournet-Mathiaud, B
- Hori, H
- Mizuta, T
- Tomé, F M
- North, K N
- Guicheney, P
Producer: 20011101
In:
Neurology vol. 57
Availability: No items available.
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13.
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134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The Netherlands. [electronic resource] by
- Bertini, E
- Burghes, A
- Bushby, K
- Estournet-Mathiaud, B
- Finkel, R S
- Hughes, R A C
- Iannaccone, S T
- Melki, J
- Mercuri, E
- Muntoni, F
- Voit, T
- Reitter, B
- Swoboda, K J
- Tiziano, D
- Tizzano, E
- Topaloglu, H
- Wirth, B
- Zerres, K
Producer: 20060207
In:
Neuromuscular disorders : NMD vol. 15
Availability: No items available.
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