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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.\par \par Callea M, Bellacchio E, Fattori F, Bertini E, Callea F, Cammarata-Scalisi F. Acute myeloid leukemia in a 3 years old child with cleidocranial dysplasia. Leuk Lymphoma 2015;:1-3.\par \par 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.\par \par 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.\par \par Montanari M, Callea M, Battelli F, Piana G. Oral rehabilitation of children with ectodermal dysplasia. BMJ Case Rep 2012;2012\par \par Callea F, Callea M. Adam's rib and the origin of stem cells. Am J Hematol 2011;86(6):529.\par \par }