Canlyniadau Chwilio - Largilliere, C

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  1. 1
    Mitochondrial very long chain acyl-CoA dehydrogenase deficiency--a new disorder of fatty acid oxidation.

    Mitochondrial very long chain acyl-CoA dehydrogenase deficiency--a new disorder of fatty acid oxidation. gan Largillière, C., Vianey-Saban, C., Fontaine, M., Bertrand, C., Kacet, N., Farriaux, J. P.

    Cyhoeddwyd 1995
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  2. 2
    Site specific screening for point mutations in ornithine transcarbamylase deficiency.

    Site specific screening for point mutations in ornithine transcarbamylase deficiency. gan Feldmann, D, Rozet, J M, Pelet, A, Hentzen, D, Briand, P, Hubert, P, Largilliere, C, Rabier, D, Farriaux, J P, Munnich, A

    Cyhoeddwyd 1992
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  3. 3
    Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.

    Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness. gan Manouvrier, S, Rötig, A, Hannebique, G, Gheerbrandt, J D, Royer-Legrain, G, Munnich, A, Parent, M, Grünfeld, J P, Largilliere, C, Lombes, A

    Cyhoeddwyd 1995
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