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Filtri: Autore è Clarich, Gabriella [Clear All Filters]
[Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia]. Arch Argent Pediatr 2015;113(6):e341-4.
. [Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia]. Arch Argent Pediatr 2017;115(1):e34-e38.
. Infantile bilateral glaucoma in a child with ectodermal dysplasia. Ophthalmic Genet 2013;34(1-2):58-60.
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