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

doi:10.1016/S0009-9120(02)00441-1

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 journal › Article › peer-review

Original language	English
Pages (from-to)	151-153
Number of pages	3
Journal	Clinical Biochemistry
Volume	36
Issue number	2
DOIs	https://doi.org/10.1016/S0009-9120(02)00441-1
Publication status	Published - Mar 2003

ASJC Scopus subject areas

Clinical Biochemistry

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10.1016/S0009-9120(02)00441-1

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

author = "Mehmet Simsek and Lihadh Al-Gazali and Reyhanah Al-Mjeni and Riad Bayoumi",

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AU - Al-Mjeni, Reyhanah

AU - Bayoumi, Riad

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

ASJC Scopus subject areas

Access to Document

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