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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).
pp. 70-78.