发明授权
US06180337B2 Diagnosis of the fragile X syndrome 失效
诊断脆性X综合征

Diagnosis of the fragile X syndrome
摘要:
A sequence of the FMR-1 gene is disclosed. This sequence and related probes, cosmids and unique repeats are used to detect X-linked diseases and especially the fragile X syndrome. Also, methods using methylation-sensitive restriction endonuclease and PCR primer probes were used to detect X-linked disease.
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