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Number of items: 2.


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, Willoughby, Cohn Eric, Camarata-Scalise, Francisco, Giovannoni, Isabelle, Vinciguerra, Agatino, Yavuz, Izzet, Di Stazio, Mariateresa, Di Iorio, Enzo, Clarich, Gabriella, Benettoni, Alessandra
et al (show 2 more authors) (2017) A c.3037G > A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype. INVESTIGACION CLINICA, 58 (1). 70 - 78.

This list was generated on Thu May 21 08:32:41 2020 BST.