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Phenotypic heterogeneity and mutational spectrum in a cohort of 45 Italian males subjects with X-linked ectodermal dysplasia.
Guazzarotti, L; Tadini, G; Mancini, G E; Giglio, S; Willoughby, C E; Callea, M; Sani, I; Nannini, P; Mameli, C; Tenconi, A A; Mauri, S; Bottero, A; Caimi, A; Morelli, M; Zuccotti, G V.
Affiliation
  • Guazzarotti L; Department of Pediatrics, University of Milan, Luigi Sacco Hospital, Milan, Italy.
Clin Genet ; 87(4): 338-42, 2015 Apr.
Article in En | MEDLINE | ID: mdl-24724966

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Ectodermal Dysplasia 1, Anhidrotic / Ectodysplasins / Mutation Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Humans / Male Country/Region as subject: Europa Language: En Journal: Clin Genet Year: 2015 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Ectodermal Dysplasia 1, Anhidrotic / Ectodysplasins / Mutation Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Humans / Male Country/Region as subject: Europa Language: En Journal: Clin Genet Year: 2015 Document type: Article Affiliation country: Country of publication: