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23. Fatal outcome in a female monozygotic twin with X-linked hypohydrotic ectodermal dysplasia (XLHED) due to a de novo t(X;9) translocation with probable disruption of the EDA gene. Zankl A; Addor MC; Cousin P; Gaide AC; Gudinchet F; Schorderet DF Eur J Pediatr; 2001 May; 160(5):296-9. PubMed ID: 11388598 [TBL] [Abstract][Full Text] [Related]
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26. [Collodion skin: a misdiagnosed but frequent clinical aspect of anhidrotic ectodermal dysplasia during the neonatal period]. Plantin P; Gavanou J; Jouan N; Leroy JP; Guillet G Ann Dermatol Venereol; 1992; 119(11):821-3. PubMed ID: 1301686 [No Abstract] [Full Text] [Related]
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30. [Christ-Siemens-Touraine syndrome in a 7-year-old boy]. Pyda E; Mastalerz Z; Darmolińska B Pediatr Pol; 1996 Mar; 71(3):261-3. PubMed ID: 8966099 [No Abstract] [Full Text] [Related]
32. Mosaic expression of hypohidrotic ectodermal dysplasia in an isolated affected female child. Bartstra HL; Hulsmans RF; Steijlen PM; Ruige M; de Die-Smulders CE; Cassiman JJ Arch Dermatol; 1994 Nov; 130(11):1421-4. PubMed ID: 7979445 [TBL] [Abstract][Full Text] [Related]
33. Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis. Zonana J; Schinzel A; Upadhyaya M; Thomas NS; Anton-Lamprecht I; Harper PS Am J Med Genet; 1990 Jan; 35(1):132-5. PubMed ID: 2301463 [TBL] [Abstract][Full Text] [Related]
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36. A dental approach to carrier screening in X linked hypohidrotic ectodermal dysplasia. Spfaer JA J Med Genet; 1981 Dec; 18(6):459-60. PubMed ID: 7334506 [TBL] [Abstract][Full Text] [Related]
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