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Browsing by Author Mencarelli, M.A.

Full Text	Issue Date	Title	Author(s)
	2009	14q12 Microdeletion syndrome and congenital variant of Rett syndrome.	Mencarelli, M.A.; Kleefstra, T.; Katzaki, E., et al
	2011	Creatine transporter defect diagnosed by proton NMR spectroscopy in males with intellectual disability	Mencarelli, M.A.; Tassini, M.; Pollazzon, M., et al
	2012	Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamics	De Filippis, R.; Pancrazi, L.; Bjorgo, K., et al
	2010	Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene.	Volpi, L.; Roversi, G.; Colombo, E.A., et al