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Find link is a tool written by Edward Betts .
Longer titles found:
Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia syndrome (view )
searching for Dentinogenesis imperfecta 5 found (192 total)
alternate case: dentinogenesis imperfecta
DMP1
(1,076 words)
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human dentin matrix acidic phosphoprotein gene (DMP1) to the dentinogenesis imperfecta type II critical region at chromosome 4q21". Genomics. 30 (2):
Osteochondrodysplasia
(2,857 words)
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identified by repeated fractures with trivial trauma, defective dentinogenesis imperfecta (DI), and hearing loss. The clinical features of COL1A1/2-related
Hall Technique
(3,421 words)
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localized or generalized i.e. in cases of enamel hypoplasia, dentinogenesis imperfecta , amelogenesis imperfecta, MIH. In patients who are at high risk
Osteopontin
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exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II". Genomics. 27 (1): 155–160. doi:10.1006/geno.1995.1018
List of OMIM disorder codes
(18,877 words)
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dysplasia, type II; 125420; DSPP Dentinogenesis imperfecta , Shields type II; 125490; DSPP Dentinogenesis imperfecta , Shields type III; 125500; DSPP Denys–Drash