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)
Original languageEnglish
Pages (from-to)151-153
Number of pages3
JournalClinical Biochemistry
Issue number2
Publication statusPublished - Mar 2003

ASJC Scopus subject areas

  • Clinical Biochemistry

Cite this