| 摘要 |
<p>An oligonucleotide or nucleic acid fragment comprising at least 17 contiguous nucleotide bases and having a sequence: (a) corresponding to at least 17 nucleotide bases of the sequence (α), (b) complementary to a sequence (a) or (c) hybridisable with a sequence (a) or (b), sequence (a) or (b) is useful for diagnosing fragile X syndrome.</p> |
