Showing results 1 to 3 of 3
Title | Author(s) | Issue Date | |
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Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese Journal:Molecular Genetics and Metabolism | 2010 | ||
2008 | |||
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome. Journal:Journal of medical genetics | 2000 |