Results
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2941.
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2942.
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2943.
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2944.
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2945.
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Peripheral and central myelinopathy in Cockayne's syndrome. Report of 3 siblings. [electronic resource] by
- Smits, M G
- Gabreëls, F J
- Renier, W O
- Joosten, E M
- Gabreëls-Festen, A A
- ter Laak, H J
- Pinckers, A J
- Hombergen, G C
- Notermans, S L
- Thijssen, H O
Producer: 19821218
In:
Neuropediatrics vol. 13
Availability: No items available.
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2946.
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2947.
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2948.
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2949.
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2950.
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Friedreich-like ataxia with retinitis pigmentosa caused by the His101Gln mutation of the alpha-tocopherol transfer protein gene. [electronic resource] by
- Yokota, T
- Shiojiri, T
- Gotoda, T
- Arita, M
- Arai, H
- Ohga, T
- Kanda, T
- Suzuki, J
- Imai, T
- Matsumoto, H
- Harino, S
- Kiyosawa, M
- Mizusawa, H
- Inoue, K
Producer: 19970710
In:
Annals of neurology vol. 41
Availability: No items available.
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2951.
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2952.
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2953.
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2954.
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2955.
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2958.
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2959.
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2960.
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