A FGFR2 mutation causing type 2 Pfeiffer syndrome

K. A. Przylepa, D. M. Moloney, S. A. Wall, D. Gagnon, G. Hoganson, M. Yin, A. O M Wilkie, E. W. Jabs

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)6-7
Number of pages2
JournalJournal of Craniofacial Genetics and Developmental Biology
Volume18
Issue number1
StatePublished - 1998

ASJC Scopus subject areas

  • Developmental Biology
  • Genetics

Cite this

Przylepa, K. A., Moloney, D. M., Wall, S. A., Gagnon, D., Hoganson, G., Yin, M., Wilkie, A. O. M., & Jabs, E. W. (1998). A FGFR2 mutation causing type 2 Pfeiffer syndrome. Journal of Craniofacial Genetics and Developmental Biology, 18(1), 6-7.