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CpG dinucleotides are mutation hot spots in phenylketonuria. [electronic resource] by
- Abadie, V
- Lyonnet, S
- Maurin, N
- Berthelon, M
- Caillaud, C
- Giraud, F
- Mattei, J F
- Rey, J
- Rey, F
- Munnich, A
Producer: 19900125
In:
Genomics vol. 5
Availability: No items available.
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37.
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Progressive muscular dystrophy. Functional improvement after a renal allograft. [electronic resource] by
- Demos, J
- Tuil, D
- Berthelon, M
- Katz, P
- Broyer, M
- Riberi, P
- Testard, R
- Rognon, L M
- Pillet, J
- Collin, P
Producer: 19770103
In:
Journal of the neurological sciences vol. 30
Availability: No items available.
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38.
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Cystic fibrosis in the population of Reunion Island. [electronic resource] by
- Hillaire, D
- Chomel, J C
- Lesure, F
- Renouil, M
- Musenger, C
- Pierson, F
- Berthelon, M
- Lenoir, G
- Gérard, G
- Bois, E
Producer: 19911204
In:
Annales de genetique vol. 34
Availability: No items available.
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39.
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A 3-base pair in-frame deletion of the phenylalanine hydroxylase gene results in a kinetic variant of phenylketonuria. [electronic resource] by
- Caillaud, C
- Lyonnet, S
- Rey, F
- Melle, D
- Frebourg, T
- Berthelon, M
- Vilarinho, L
- Vaz Osorio, R
- Rey, J
- Munnich, A
Producer: 19910625
In:
The Journal of biological chemistry vol. 266
Availability: No items available.
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40.
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[Phenotypic expression of 12 mutations of the phenylalanine hydroxylase gene]. [electronic resource] by
- Rey, F
- Abadie, V
- Lyonnet, S
- Berthelon, M
- Caillaud, C
- Melle, D
- Labrune, P
- Saudubray, J M
- Munnich, A
- Rey, J
Producer: 19930312
In:
Archives francaises de pediatrie vol. 49
Availability: No items available.
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