Cinzia Magnani

Stickler syndrome caused by COL2A1 mutations: genotype–phenotype correlation in a series of 100 patients

Kristien Hoornaert, Inge Vereecke, Chantal Dewinter et al. · European Journal of Human Genetics · 2010 · 147 citations · Full text

Mendelian Disorder, Autoimmune Disease, Genetic Disorder +11

FAM111A Mutations Result in Hypoparathyroidism and Impaired Skeletal Development

Sheila Unger, Maria W. Górna, Antony Le Béchec et al. · The American Journal of Human Genetics · 2013 · 136 citations · Full text

Bone Disease, Developmental Biology, Mendelian Disorder +5

Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome

Saskia M. Maas, Adam Shaw, Hennie Bikker et al. · European Journal of Medical Genetics · 2015 · 119 citations · Full text

Tricho-rhino-phalangeal Syndrome, Genetics, Genetic Epidemiology +1

Italian cancer figures, report 2012: Cancer in children and adolescents.

Paola Pisani, Carlotta Buzzoni, Emanuele Crocetti et al. · BOA (University of Milano-Bicocca) · 2013 · 118 citations

Congenital heart defects: 15 years of experience of the Emilia-Romagna Registry (Italy)

Elisa Calzolari, Giampaolo Garani, G Cocchi et al. · European Journal of Epidemiology · 2003 · 97 citations

Heart Failure, Congenital Heart Defects, Emilia-romagna Registry +9