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

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)151-153
Number of pages3
JournalClinical Biochemistry
Volume36
Issue number2
DOIs
Publication statusPublished - Mar 2003

ASJC Scopus subject areas

  • Clinical Biochemistry

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