HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

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

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.
AuthorsM Nakata, H Koshiba, K Eto, W E Nance
JournalAmerican journal of human genetics (Am J Hum Genet) Vol. 32 Issue 6 Pg. 908-19 (Nov 1980) ISSN: 0002-9297 [Print] United States
PMID7446529 (Publication Type: Journal Article)
Topics
  • Anodontia (genetics)
  • Dentition
  • Ectodermal Dysplasia (diagnosis, genetics)
  • Female
  • Genes, Recessive
  • Genetic Carrier Screening
  • Genetic Linkage
  • Humans
  • Male
  • Odontometry
  • Pedigree
  • Sex Chromosomes
  • Tooth Abnormalities (genetics)
  • X Chromosome

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: