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Autore Titolo Tipo [ Anno(Asc)]
Filtri: Autore è Clarich, Gabriella  [Clear All Filters]
2017
Callea M, Cammarata-Scalisi F, Willoughby CE, Giglio SR, Sani I, Bargiacchi S, Traficante G, Bellacchio E, Tadini G, Yavuz I, Galeotti A, Clarich G. [Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia]. Arch Argent Pediatr 2017;115(1):e34-e38.
2015
Callea M, Yavuz I, Clarich G, Cammarata-Scalisi F. [Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia]. Arch Argent Pediatr 2015;113(6):e341-4.
2013
Callea M, Vinciguerra A, Willoughby CE, Deroma L, Clarich G. Infantile bilateral glaucoma in a child with ectodermal dysplasia. Ophthalmic Genet 2013;34(1-2):58-60.

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