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Journal List > Am J Hum Genet > v.32(6); Nov 1980

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Am J Hum Genet. 1980 November; 32(6): 908–919.
PMCID: PMC1686146
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A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia.
M Nakata, H Koshiba, K Eto, and W E Nance
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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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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
  • SEAGLE JB. Anhidrotic hereditary ectodermal dysplasia; report of two cases in a brother and sister. J Pediatr. 1954 Dec;45(6):688–691. [PubMed]
  • Passarge E, Nuzum CT, Schubert WK. Anhidrotic ectodermal dysplasia as autosomal recessive trait in an inbred kindred. Humangenetik. 1966;3(2):181–185. [PubMed]
  • Kratzsch R. Ektodermale Dysplasie vom anhidrotischen Typ bei zwei Schwestern. Klin Padiatr. 1972 Jul;184(4):328–332. [PubMed]
  • Kerr CB, Wells RS, Cooper KE. Gene effect in carriers of anhidrotic ectodermal dysplasia. J Med Genet. 1966 Sep;3(3):169–176. [PMC free article] [PubMed]
  • Frias JL, Smith DW. Diminished sweat pores in hypohidrotic ectodermal dysplasia: a new method for assessment. J Pediatr. 1968 May;72(5):606–610. [PubMed]
  • Carter WJ, Bordy MD. Ectodermal dysplasia and the Lyon hypothesis. J Dent Child. 1967 Jul;34(4):265–268. [PubMed]
  • Bailit HL. Dental variation among populations. An anthropologic view. Dent Clin North Am. 1975 Jan;19(1):125–139. [PubMed]
  • GARN SM, LEWIS AB, VICINUS JH. Third molar agenesis and reduction in the number of other teeth. J Dent Res. 1962 May–Jun;41:717. [PubMed]
  • Francke U, Felsenstein J, Gartler SM, Migeon BR, Dancis J, Seegmiller JE, Bakay F, Nyhan WL. The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease. Am J Hum Genet. 1976 Mar;28(2):123–137. [PMC free article] [PubMed]
  • Francke U, Felsenstein J, Gartler SM, Nyhan WL, Seegmiller JE. Answer to criticism of Morton and Lalouel. Am J Hum Genet. 1977 May;29(3):307–311. [PMC free article] [PubMed]
  • Morton NE, Lalouel JM. Genetic epidemiology of Lesch-Nyhan disease. Am J Hum Genet. 1977 May;29(3):304–311. [PMC free article] [PubMed]
  • Pickard NA, Gruemer HD, Verrill HL, Isaacs ER, Robinow M, Nance WE, Myers EC, Goldsmith B. Systemic membrane defect in the proximal muscular dystrophies. N Engl J Med. 1978 Oct 19;299(16):841–846. [PubMed]
  • Kaplan E, Shwachman H, Perlmutter AD, Rule A, Khaw KT, Holsclaw DS. Reproductive failure in males with cystic fibrosis. N Engl J Med. 1968 Jul 11;279(2):65–69. [PubMed]
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