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Establishment of a Nonradioactive Molecular Diagnosis of Fragile-X Syndrome
Lp(a) coronary artery disease dot blot analysis DIG-labeling apo(a) gene
2009/6/30
Fragile-X syndrome is a hereditary dynamic mutation disorder, predominantly caused by a large expansion of CGG trinucleotide repeats in the FMR 1 gene leading to methylation and down regulation of tra...
Molecular diagnosis for presymptomatic patients with Wilson disease
Wilson disease ATP7B gene analysis presymptomatic diagnosis
2009/4/1
Wilson disease is a genetic disorder of copper metabolism characterized by hepatic and/or neurological manifestations. This disease is caused by mutations in the gene of copper transporting ATPase (AT...
Significance of Molecular Diagnosis using Histopathological Specimens in Cestode Zoonoses
Cestode zoonoses mitochondrial DNA analysis histopathological specimens
2010/12/10
Cestode zoonosis cases confirmed by PCR-based mitochondrial DNA analysis were investigated. The cestodiosis included taeniasis, cysticercosis, alveolar echinococcosis, cystic echinococcosis, sparganos...