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Clinical Genetics|February 5, 2005
Germline mosaicism in Rett syndrome identified by prenatal diagnosisF Mari, R Caselli, S Russo, et al.Plos One|May 22, 2013
Trends in the prevalence of tuberous sclerosis complex manifestations: an epidemiological study of 166 Japanese patientsMari Wataya-Kaneda, Mari Tanaka, Toshimitsu Hamasaki, et al.Hepato-Gastroenterology|December 1, 1983
Serum pancreatic enzyme alterations in acute viral hepatitisA Lechi, G Montesi, M Solbiati, et al.Nano Letters|December 14, 2006
High-performance transparent conducting oxide nanowiresQing Wan, Eric N Dattoli, Wayne Y Fung, et al.Human Mutation|December 23, 2006
Italian Rett database and biobankKatia Sampieri, Ilaria Meloni, Elisa Scala, et al.American Journal of Medical Genetics. Part A|October 31, 2007
MECP2 deletions and genotype-phenotype correlation in Rett syndromeElisa Scala, Ilaria Longo, Federica Ottimo, et al.American Journal of Medical Genetics. Part A|July 16, 2008
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like featuresFilomena Tiziana Papa, Maria Antonietta Mencarelli, Rossella Caselli, et al.The Journal of Cell Biology|April 25, 2020
Asymmetric assembly of centromeres epigenetically regulates stem cell fateAnna Ada Dattoli, Ben L Carty, Antje M Kochendoerfer, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 13, 2005
Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five familiesIlaria Longo, Elisa Scala, Francesca Mari, et al.Journal of Submicroscopic Cytology and Pathology|April 1, 1989
Localization of acrosomal enzymes in Arthropoda, Echinodermata and VertebrataB Baccetti, A G Burrini, G Collodel, et al.Pageof 2,644