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Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta
Author(s) -
Hart PS,
Becerik S,
Cogulu D,
Emingil G,
OzdemirOzenen D,
Han ST,
Sulima PP,
Firatli E,
Hart TC
Publication year - 2009
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2008.01112.x
Subject(s) - amelogenesis imperfecta , craniofacial , library science , medicine , turkish , family medicine , dentistry , psychiatry , linguistics , philosophy , enamel paint , computer science