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 journalArticlepeer-review

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

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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