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Dentinogenesis Imperfecta 1

Dentinogenesis imperfecta - Shield's type II
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Review Articles from PubMed

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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Dentinogenesis Imperfecta 1" returned 0 free, full-text research articles. First 0 results:
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.
Last Updated: Feb 05, 2010

Dentinogenesis imperfecta 1 (DGI1, MIM 125490) is an autosomal dominant dental disease characterized by abnormal dentin production and mineralization. The DGI1 locus was recently refined to a 2-Mb interval on 4q21 (ref. 1). Here we study three Chinese families carrying DGI1. We find ...

Elucidation of the sequence and the genomic organization of the human dentin matrix acidic phosphoprotein 1 (DMP1) gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II.
Last Updated: Sep 29, 2009

The dentin matrix acidic phosphoprotein 1 (DMP1) gene has been mapped to human chromosome 4q21 and shown to exhibit no recombination with the autosomal dominant disorder of dentin formation, dentinogenesis imperfecta type II. In the current study, sequencing of DMP1 cDNA and genomic ...

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