Adelaide Research & Scholarship
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Total Visits
| Views | |
|---|---|
| A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome(legacy) | 108 |
| A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome(legacy) | 61 |
Total Visits per Month
| April 2022 | May 2022 | June 2022 | July 2022 | August 2022 | September 2022 | October 2022 | |
|---|---|---|---|---|---|---|---|
| A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome | 0 | 2 | 2 | 0 | 3 | 0 | 0 |
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