Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia

M. Callea, F. Cammarata-Scalisi, C.E. Willoughby, S.R. Giglio, Dra.I. Sani, S. Bargiacchi, G. Traficante, E. Bellacchio, G. Tadini, I. Yavuz, A. Galeotti, G. Clarich

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)e34-e38
JournalArchivos Argentinos de Pediatria
Volume115
Issue number1
DOIs
Publication statusPublished - 2017

Cite this

Callea, M., Cammarata-Scalisi, F., Willoughby, C. E., Giglio, S. R., Sani, D. I., Bargiacchi, S., ... Clarich, G. (2017). Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia. Archivos Argentinos de Pediatria, 115(1), e34-e38. https://doi.org/10.5546/aap.2017.e34