Diagnosis Of The Fragile X Syndrome

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Abstract

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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Document History
  • Publication: Jan 30, 2001
  • Application: Aug 29, 1991
    US US 75189191 A
  • Priority: Aug 29, 1991
    US US 75189191 A
  • Priority: May 24, 1991
    US US 70549091 A

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