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Logo of procrsmedFormerly medchtJournal of the Royal Society of MedicineProceedings of the Royal Society of Medicine
 
Proc R Soc Med. 1958 September; 51(9): 707–712.
PMCID: PMC1889807

Cases

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • Clouston HR. THE MAJOR FORMS OF HEREDITARY ECTODERMAL DYSPLASIA : (With an Autopsy and Biopsies on the Anhydrotic Type). Can Med Assoc J. 1939 Jan;40(1):1–7. [PMC free article] [PubMed]
  • OSBOURN RA. Congenital ectodermal defect with amastia. J Am Med Assoc. 1952 Feb 23;148(8):644–645. [PubMed]
  • UPSHAW BY, MONTGOMERY H. Hereditary anhidrotic ectodermal dysplasia, a clinical and pathologic study. Arch Derm Syphilol. 1949 Dec;60(6):1170–illust. [PubMed]
  • COLE HN, RAUSCHKOLB J, TOOMEY J. Dyskeratosis congenita with pigmentation, dystrophia unguium, and leucokeratosis oris; review of the known cases reported to date and discussion of the disease from various aspects. AMA Arch Derm. 1955 Apr;71(4):451–456. [PubMed]
  • PEGUM JS. Diffuse pigmentation in brothers. Proc R Soc Med. 1955 Mar;48(3):179–180. [PubMed]
  • PEGUM JS. Diffuse pigmentation in brothers. Proc R Soc Med. 1955 Mar;48(3):179–180. [PubMed]

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