A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia - PubMed (original) (raw)

• PMID: 7446529
• PMCID: PMC1686146

A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia

M Nakata et al. Am J Hum Genet. 1980 Nov.

Abstract

Dental examinations and tooth measurements were conducted on 16 mothers, 10 fathers, and 23 affected males in 15 families with X-linked hypohidrotic ectodermal dysplasia. Small teeth and congenital missing teeth were sufficiently consistent findings in obligate heterozygotes to suggest that carriers can usually be recognized by clinical criteria.

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