Dentin dysplasia, type II linkage to chromosome 4q.

Article

Dentin dysplasia, type II linkage to chromosome 4q.

Journal of craniofacial genetics and developmental biology - 1 Jan 2000

Dean J A, Hartsfield J K, Wright J T, Hart T C

Abstract excerpt

Dentin dysplasia, type II (MIM*125420) is an autosomal dominant disorder of dentin development. Clinically the primary dentition appears opalescent, and radiographically the pulp chambers are obliterated, resembling dentinogenesis imperfecta. However, unlike dentinogenesis imperfecta, the permane...

Topics

Alleles
Chromosomes, Human, Pair 4
Dentin Dysplasia
Dentinogenesis Imperfecta
Female
Genes, Dominant
Genetic Linkage
Genotype
Humans
Lod Score
Male
Microsatellite Repeats
Pedigree
Tooth Abnormalities

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