Variants of ST8SIA1 Are Associated with Risk of Developing Multiple Sclerosis

Por Husain, Seema, Yildirim-Toruner, Cagri, Rubio, Justin P., Field, Judith, Schwalb, Marvin, Cook, Stuart, Devoto, Marcella, Vitale, Emilia
Publicado em 2008

Donor Splice-Site Mutation in CUL4B is Likely Cause of X-Linked Intellectual Disability

Por Londin, Eric R., Adijanto, Jeffrey, Philp, Nancy, Novelli, Antonio, Vitale, Emilia, Perria, Chiara, Serra, Gigliola, Alesi, Viola, Surrey, Saul, Fortina, Paolo
Publicado no Am J Med Genet A (2014)

Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms in Italian families: A collaborative study

Por Estivill, Xavier, Farrall, Martin, Williamson, Robert, Ferrari, Maurizio, Seia, Manuela, Giunta, Anna Maria, Novelli, Giuseppe, Potenza, Lucia, Dallapicolla, Bruno, Borgo, Graziella, Gasparini, Paolo, Pignatti, Pier F., De Benedetti, Laura, Vitale, Emilia, Devoto, Marcella, Romeo, Giovanni
Publicado em 1988