Showing results 21 to 24 of 24
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Title | Author(s) | Issue Date | |
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A novel mutation of SLC22A12 gene causing primary renal hypouricemia in a patient with metabolic syndrome Journal:Clinica Chimica Acta | 2008 | ||
Novel mutations in myopathic form of carnitine palmitoyltransferase II deficiency in a Chinese patient Journal:Clinica Chimica Acta | 2013 | ||
Role of postmortem genetic testing demonstrated in a case of glutaric aciduria type II Journal:Diagnostic Molecular Pathology | 2010 | ||
The variability of the hepatitis B virus genome: Statistical analysis and biological implications Journal:Molecular Biology and Evolution | 1993 |