Identification of FGFR3 mutations in 28 achondroplasia patients, in 10 of 18 cases of hypochodroplasia and in both cases with type I TD, is reported here. To detect mutations of achondroplasia, both natural restriction site and amplification created restriction site (ACRS) were utilized. Mutation 11
Somatic mutations of fibroblast growth factor receptor 3 (FGFR3) are uncommon in carcinomas of the uterine cervix
✍ Scribed by Wu, Rong; Connolly, Denise; Ngelangel, Cora; Bosch, F Xavier; Muñoz, Nubia; Cho, Kathleen R
- Book ID
- 110064246
- Publisher
- Nature Publishing Group
- Year
- 2000
- Tongue
- English
- Weight
- 168 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0950-9232
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