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32. Diffuse Palmoplantar Keratoderma, Onychodystrophy, universal Hypotrichosis and Cysts. Arif T; Amin SS; Adil M; Mohtashim M Acta Dermatovenerol Croat; 2017 Jul; 25(2):161-163. PubMed ID: 28871934 [TBL] [Abstract][Full Text] [Related]
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34. Mutation in the ED1 gene, Ala349Thr, in a Korean patient with X-linked hypohidrotic ectodermal dysplasia developing de novo. Na GY; Kim DW; Lee SJ; Chung SL; Park DJ; Kim JC; Kim MK Pediatr Dermatol; 2004; 21(5):568-72. PubMed ID: 15461765 [TBL] [Abstract][Full Text] [Related]
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38. A new autosomal dominant syndrome of hypohidrotic ectodermal dysplasia and unusual facies. Bocian M; Rimoin DL Birth Defects Orig Artic Ser; 1979; 15(5B):239-51. PubMed ID: 526580 [No Abstract] [Full Text] [Related]
40. Ozena as presenting symptom of a rare and severe genetic disease: hypohidrotic ectodermal dysplasia. Martini A; Magnan G; Peserico A Int J Pediatr Otorhinolaryngol; 1984 Oct; 8(1):97-103. PubMed ID: 6500829 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]