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Cammarata-Scalisi, Francisco, Willoughby, Colin Eric, Romano, Vito 
ORCID: 0000-0002-5148-7643 and Callea, Michele
(2023)
Challenges in Communicating a Genetic Diagnosis.
CHILDREN-BASEL, 10 (4).
672-.
Callea, Michele, Cammarata-Scalisi, Francisco, Willoughby, Colin E, Giglio, Sabrina R, Sani, Ilaria, Bargiacchi, Sara, Traficante, Giovanna, Bellacchio, Emanuele, Tadini, Gianluca, Yavuz, Izzet et al (show 2 more authors)
(2017)
Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia.
ARCHIVOS ARGENTINOS DE PEDIATRIA, 115 (1).
E34-E38.
Callea, Michele, Bignotti, Stefano, Semeraro, Francesco, Cammarata-Scalisi, Francisco, El-Feghaly, Jinia, Morabito, Antonino, Romano, Vito ORCID: 0000-0002-5148-7643 and Willoughby, Colin E
(2022)
Extended Overview of Ocular Phenotype with Recent Advances in Hypohidrotic Ectodermal Dysplasia.
CHILDREN-BASEL, 9 (9).
1357-.