A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia.

A. Giannotti, A. Tessa, C. Patrono, L. D. Florio, M. Velardo, C. Dionisi-Vici, E. Bertini, F. M. Santorelli

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)277
Number of pages1
JournalHuman Mutation
Volume16
Issue number3
Publication statusPublished - Sep 2000

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Giannotti, A., Tessa, A., Patrono, C., Florio, L. D., Velardo, M., Dionisi-Vici, C., Bertini, E., & Santorelli, F. M. (2000). A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia. Human Mutation, 16(3), 277.