Showing results 15 to 24 of 24
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Title | Author(s) | Issue Date | Views | |
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Lathosterolosis: A Disorder Of Cholesterol Biosynthesis Resembling Smith-lemli-opitz Syndrome Journal:Journal Of Inherited Metabolic Disease | 2014 | 84 | ||
2012 | 81 | |||
Neurocognitive evaluation and plasma clozapine concentrations in Chinese patients with treatment-refractory schizophrenia Proceeding/Conference:International Journal of Neuropsychopharmacology | 2002 | 143 | ||
2012 | 198 | |||
2010 | 149 | |||
2007 | ||||
A novel mutation of SLC22A12 gene causing primary renal hypouricemia in a patient with metabolic syndrome Journal:Clinica Chimica Acta | 2008 | 189 | ||
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 | 141 | ||
The variability of the hepatitis B virus genome: Statistical analysis and biological implications Journal:Molecular Biology and Evolution | 1993 |