The fragile X syndrome is due to an expansion of the CGG trinucleotide repeat in the FMR1 gene and hypermethylation of its 5 upstream CpG island in about 95% of the cases. The remaining 5% of cases correspond to other molecular alterations in FMR1 gene such as partial or complete deletions, or point
✦ LIBER ✦
Gene Mapping in Zebrafish Using Single-Strand Conformation Polymorphism Analysis
✍ Scribed by Dorothee Förnzler; Helen Her; Ela W. Knapik; Matthew Clark; Hans Lehrach; John H. Postlethwait; Leonard I. Zon; David R. Beier
- Book ID
- 115614382
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 155 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0888-7543
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