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A novel form of familial congenital muscular dystrophy in two adolescents. [electronic resource] by
- Salih, M A
- Al Rayess, M
- Cutshall, S
- Urtizberea, J A
- Al-Turaiki, M H
- Ozo, C O
- Straub, V
- Akbar, M
- Abid, M
- Andeejani, A
- Campbell, K P
Producer: 19990524
In:
Neuropediatrics vol. 29
Availability: No items available.
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12.
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A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23. [electronic resource] by
- Gribaa, M
- Salih, M
- Anheim, M
- Lagier-Tourenne, C
- H'mida, D
- Drouot, N
- Mohamed, A
- Elmalik, S
- Kabiraj, M
- Al-Rayess, M
- Almubarak, M
- Bétard, C
- Goebel, H
- Koenig, M
Producer: 20070724
In:
Brain : a journal of neurology vol. 130
Availability: No items available.
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13.
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Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity. [electronic resource] by
- Salih, M A
- Maisonobe, T
- Kabiraj, M
- al Rayess, M
- al-Turaiki, M H
- Akbar, M
- Tahan, A
- Urtizberea, J A
- Grid, D
- Hamadouche, T
- Guilbot, A
- Brice, A
- Leguern, E
Producer: 20000307
In:
Neuromuscular disorders : NMD vol. 10
Availability: No items available.
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