Showing results 1 to 5 of 5
Title | Author(s) | Issue Date | |
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Diagnosis of dihydropyrimidine dehydrogenase deficiency in a neonate with thymine-uraciluria Journal:Hong Kong Medical Journal | 2003 | ||
Diagnostic value of pleural fluid adenosine deaminase activity in tuberculous pleurisy Journal:Clinica Chimica Acta | 2004 | ||
Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome: a treatable genetic liver disease warranting urgent diagnosis Journal:Hong Kong Medical Journal | 2014 | ||
Novel missense mutation (Y279S) in the GLRA1 gene causing hyperekplexia [2] Journal:Clinica Chimica Acta | 2006 | ||
Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activity Journal:Clinica Chimica Acta | 2005 |