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

TitoloA novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia.
Tipo di pubblicazioneArticolo su Rivista peer-reviewed
Anno di Pubblicazione2000
AutoriGiannotti, A., Tessa A., Patrono Clarice, Florio L.D., Velardo M., Dionisi-Vici C., Bertini E., and Santorelli F.M.
RivistaHuman mutation
Volume16
Paginazione277
ISSN10981004
Note

cited By 9

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0034267570&doi=10.1002%2f1098-1004%28200009%2916%3a3%3c277%3a%3aAID-HUMU25%3e3.0.CO%3b2-V&partnerID=40&md5=94ec87b2a6f3ef975b4dedfa1387fbd2
DOI10.1002/1098-1004(200009)16:3<277::AID-HUMU25>3.0.CO;2-V
Citation KeyGiannotti2000277