Angela Spalletta

Familial 1.1 Mb deletion in chromosome Xq22.1 associated with mental retardation and behavioural disorders in female patients

Lucia Grillo, S Reitano, Giovanni Belfiore et al. · European Journal of Medical Genetics · 2010 · 95 citations

Life Sciences, Genetics, Molecular Genetics +14

<i>CDKL5</i> mutations in boys with severe encephalopathy and early-onset intractable epilepsy

Maurizio Elia, M.L. Ruiz Falcó, Raffaele Ferri et al. · Neurology · 2008 · 90 citations

Life Sciences, Genetics, Neurology +17

1.5 Mb<i> de novo </i>22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features

A Alberti, Corrado Romano, M. Falco et al. · Clinical Genetics · 2007 · 55 citations

Life Sciences, Genetics, Craniofacial Genetics +15

Increased FGF3 and FGF4 gene dosage is a risk factor for craniosynostosis

Lucia Grillo, Donatella Greco, Rosa Pettinato et al. · Gene · 2013 · 23 citations

Dentistry, Craniofacial Biology, Developmental Biology +12

Molecular basis of α-thalassemia in Sicily

Marco Fichera, Angela Spalletta, Flavia Fiorenza et al. · Human Genetics · 1997 · 22 citations

Medicine, Genetics, Molecular Genetics +6