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Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation. [electronic resource] by
- Herman-Bert, A
- Stevanin, G
- Netter, J C
- Rascol, O
- Brassat, D
- Calvas, P
- Camuzat, A
- Yuan, Q
- Schalling, M
- Dürr, A
- Brice, A
Producer: 20000807
In:
American journal of human genetics vol. 67
Availability: No items available.
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51.
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Statistical analysis of mitochondrial pathologies in childhood: identification of deficiencies using principal component analysis. [electronic resource] by
- Letellier, T
- Durrieu, G
- Malgat, M
- Rossignol, R
- Antoch, J
- Deshouillers, J M
- Coquet, M
- Lacombe, D
- Netter, J C
- Pedespan, J M
- Redonnet-Vernhet, I
- Mazat, J P
Producer: 20000801
In:
Laboratory investigation; a journal of technical methods and pathology vol. 80
Availability: No items available.
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52.
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Severe lactic acidosis and acute thiamin deficiency: a report of 11 neonates with unsupplemented total parenteral nutrition. [electronic resource] by
- Thauvin-Robinet, C
- Faivre, L
- Barbier, M L
- Chevret, L
- Bourgeois, J
- Netter, J C
- Grimaldi, M
- Geneviève, D
- Ogier de Baulny, H
- Huet, F
- Saudubray, J M
- Gouyon, J B
Producer: 20050324
In:
Journal of inherited metabolic disease vol. 27
Availability: No items available.
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