Cutaneous findings in sporadic and familial autosomal dominant hyper-IgE syndrome: A retrospective, single-center study of 21 patients diagnosed using molecular analysis.
Autor: | Olaiwan A, Chandesris MO, Fraitag S, Lortholary O, Hermine O, Fischer A, de Prost Y, Picard C, Bodemer C |
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Zdroj: | Journal of the American Academy of Dermatology; Dec2011, Vol. 65 Issue 6, p1167-1172, 6p |
Databáze: | Supplemental Index |
Externí odkaz: |