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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...