Improved diagnosis of a common mutation (R248C) in the human growth factor receptor 3 (FGFR3) gene that causes type I Thanatophoric dysplasia

Mehmet Simsek, Lihadh Al-Gazali, Reyhanah Al-Mjeni, Riad Bayoumi

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)

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