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L-2-hydroxyglutaric aciduria: two further cases. [electronic resource] by
- Divry, P
- Jakobs, C
- Vianey-Saban, C
- Gibson, K M
- Michelakakis, H
- Papadimitriou, A
- Divari, R
- Chabrol, B
- Cournelle, M A
- Livet, M O
Producer: 19950817
In:
Journal of inherited metabolic disease vol. 16
Availability: No items available.
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9.
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Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes. [electronic resource] by
- Tezenas du Montcel, S
- Clot, F
- Vidailhet, M
- Roze, E
- Damier, P
- Jedynak, C P
- Camuzat, A
- Lagueny, A
- Vercueil, L
- Doummar, D
- Guyant-Maréchal, L
- Houeto, J-L
- Ponsot, G
- Thobois, S
- Cournelle, M-A
- Durr, A
- Durif, F
- Echenne, B
- Hannequin, D
- Tranchant, C
- Brice, A
Producer: 20060717
In:
Journal of medical genetics vol. 43
Availability: No items available.
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