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Paper Details

A Novel <i>AMELX</i> Mutation, Its Phenotypic Features, and Skewed X Inactivation.
J Dent Res
10
2019
AI, AMELX, AMELX Mutation, AMELX mutations, Amelogenesis imperfecta, T, X, X chromosome, X-linked AI, amelogenin, androgen, androgen receptor allele, c, exon 5, genetic disorders, hypoplastic and hypomineralized AI, maternal, maternal tooth, peripheral, peripheral blood DNA, polymerase chain reaction products
Author NameAffiliation
Cornelius F BoerkoelUniversity of British Columbia
Cornelius F BoerkoelUniversity of British Columbia
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