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Browsing by Author Renieri, A.

Full Text	Issue Date	Title	Author(s)
	2011	Creatine transporter defect diagnosed by proton NMR spectroscopy in males with intellectual disability	Mencarelli, M.A.; Tassini, M.; Pollazzon, M.; Vivi, A.; Calderisi, M., et al
	2009	14q12 Microdeletion syndrome and congenital variant of Rett syndrome.	Mencarelli, M.A.; Kleefstra, T.; Katzaki, E.; Papa, F.T.; Cohen, M., et al
	2008	Mutational spectrum of the oral-facial-digital type I syndrome: a study on a large collection of patients.	Prattichizzo, C.; Macca, M.; Novelli, V.; Giorgio, G.; Barra, A., et al