BACCARIN, MARCO
BACCARIN, MARCO
Universita' degli Studi di MILANO
Huntingtin gene CAG repeat size affects autism risk: Family-based and case–control association study
2020 I.S. Piras, C. Picinelli, R. Iennaco, M. Baccarin, P. Castronovo, P. Tomaiuolo, F. Cucinotta, A. Ricciardello, L. Turriziani, L. Nanetti, C. Mariotti, C. Gellera, C. Lintas, R. Sacco, C. Zuccato, E. Cattaneo, A.M. Persico
Prenatal upper-limb mesomelia and 2q31.1 microdeletions affecting the regulatory genome
2018 A. Peron, S. Boito, T. Rizzuti, I. Borzani, M. Baccarin, M.F. Bedeschi, F. Lalatta
New Insights into Kleefstra Syndrome : Report of Two Novel Cases with Previously Unreported Features and Literature Review
2018 C. Ciaccio, G. Scuvera, A. Tucci, B. Gentilin, M. Baccarin, P. Marchisio, S. Avignone, D. Milani
7p22.1 microduplication syndrome : refinement of the critical region
2017 L. Ronzoni, F.S. Grassi, L. Pezzani, A. Tucci, M. Baccarin, S. Esposito, D. Milani
Sequence variants identification at the KCNQ1OT1: TSS differentially Methylated region in isolated omphalocele cases
2017 B. Maria Francesca, M. Calvello, L. Paganini, L. Pezzani, M. Baccarin, L. Fontana, S.M. Sirchia, G. Silvana, L. Canazza, L. Ernesto, L.L. Colombo, L. Faustina, F. Mosca, S.M. Tabano, M.R. Miozzo
Rare interstitial deletion of chromosome 2p11.2p12 : Report of a new patient with developmental delay and unusual clinical features
2016 R. Silipigni, E. Cattaneo, M. Baccarin, M. Fumagalli, M.F. Bedeschi
Impaired Angiogenic Potential of Human Placental Mesenchymal Stromal Cells in Intrauterine Growth Restriction
2016 C. Mandò, P. Razini, C. Novielli, G.M. Anelli, M. Belicchi, S. Erratico, S. Banfi, M. Meregalli, A. Tavelli, M. Baccarin, A. Rolfo, S. Motta, Y. Torrente, I. Cetin
Insights into 6q21-q22 : Refinement of the critical region for acro-cardio-facial syndrome
2016 D. Milani, G.A. Cagnoli, M. Baccarin, E. Alfei, S. Guerneri, S. Esposito
HOXA genes cluster: clinical implications of the smallest deletion
2015 L. Pezzani, D. Milani, F. Manzoni, M. Baccarin, R. Silipigni, S. Guerneri, S. Esposito
Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins : a genotype-phenotype analysis
2015 L. Ronzoni, A. Peron, V. Bianchi, M. Baccarin, S. Guerneri, R. Silipigni, F. Lalatta, M.F. Bedeschi