Associated Papers
Insights into Hyperparathyroidism-Jaw Tumour Syndrome: From Endocrine Acumen to the Spectrum of CDC73 Gene and Parafibromin-Deficient Tumours.
Gheorghe AM et al.
International Journal of Molecular Sciences, 2024
Endothelial nitric oxide synthase 894G→T but not -786T→C gene polymorphism is associated with organ dysfunction and increased mortality in patients with severe sepsis.
Ma P et al.
The Journal of Trauma, 2011
Molecular diagnosis of primary hyperparathyroidism in familial cancer syndromes.
Marsh DJ et al.
Expert Opinion on Medical Diagnostics, 2007
Distinct mechanisms lead to HPRT gene mutations in leukemic cells.
Lin YW et al.
Genes, Chromosomes & Cancer, 2004
Pyrosequencing technology as a method for the diagnosis of multiple endocrine neoplasia type 2.
Kruckeberg KE et al.
Clinical Chemistry, 2004
Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1.
Eng C et al.
Journal of Medical Genetics, 2001
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