Marzia Pollazzon
Azienda Sanitaria Unità Locale di Reggio Emilia(IT)Istituti di Ricovero e Cura a Carattere Scientifico(IT)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, Congenital heart defects research, Connective tissue disorders research
Most-Cited Works
- → FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome(2008)432 cited
- → Private inherited microdeletion/microduplications: Implications in clinical practice(2008)106 cited
- → Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care(2018)105 cited
- → Early-onset seizure variant of Rett syndrome: Definition of the clinical diagnostic criteria(2009)72 cited
- → The first Italian family with tibial muscular dystrophy caused by a novel titin mutation(2009)55 cited
- → Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients(2016)55 cited
- → Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation