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E Ploechl

Showing results (1-10 of 4) with videos related to

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The Journal of International Medical Research|January 1, 1986
Clinical experience with intravenous Augmentin in the treatment of paediatric infectionsE Ploechl, E G Huber
Clinical Genetics|March 22, 2001
Late-onset ornithine transcarbamylase deficiency in two families with different mutations in the same codonE Ploechl, W Ploechl, S Stoeckler-Ipsiroglu, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Outcome of tyrosinaemia type IIIC J Ellaway, E Holme, S Standing, et al.
Molecular Genetics and Metabolism|November 14, 2000
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuriaK Tomoeda, H Awata, T Matsuura, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
The Journal of International Medical Research|January 1, 1986
Clinical experience with intravenous Augmentin in the treatment of paediatric infectionsE Ploechl, E G Huber
Clinical Genetics|March 22, 2001
Late-onset ornithine transcarbamylase deficiency in two families with different mutations in the same codonE Ploechl, W Ploechl, S Stoeckler-Ipsiroglu, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Outcome of tyrosinaemia type IIIC J Ellaway, E Holme, S Standing, et al.
Molecular Genetics and Metabolism|November 14, 2000
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuriaK Tomoeda, H Awata, T Matsuura, et al.
Pageof 1