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3. An autosomal recessive ectodermal dysplasia syndrome of hypotrichosis, onychodysplasia, hyperkeratosis, kyphoscoliosis, catartact, and other manifestations. Alves AF; dos Santos PA; Castelo-Branco-Neto E; Freire-Maia N Am J Med Genet; 1981; 10(3):213-8. PubMed ID: 7304669 [TBL] [Abstract][Full Text] [Related]
5. Clinical management of hypohidrotic ectodermal dysplasia with anodontia: case report. Paschos E; Huth KC; Hickel R J Clin Pediatr Dent; 2002; 27(1):5-8. PubMed ID: 12413164 [TBL] [Abstract][Full Text] [Related]
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18. A distinctive type of hypohidrotic ectodermal dysplasia featuring hypothyroidism. Pike MG; Baraitser M; Dinwiddie R; Atherton DJ J Pediatr; 1986 Jan; 108(1):109-11. PubMed ID: 3944674 [No Abstract] [Full Text] [Related]
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20. Prevalence and prevention of severe complications of hypohidrotic ectodermal dysplasia in infancy. Blüschke G; Nüsken KD; Schneider H Early Hum Dev; 2010 Jul; 86(7):397-9. PubMed ID: 20682465 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]