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Titolo Data di pubblicazione Autori Tipo File Abstract
Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins : a genotype-phenotype analysis 2015 L. RonzoniA. PeronM. BaccarinR. Silipigni + Article (author) -
HOXA genes cluster: clinical implications of the smallest deletion 2015 L. PezzaniD. MilaniF. ManzoniM. BaccarinR. SilipigniS. Esposito + Article (author) -
Rare interstitial deletion of chromosome 2p11.2p12 : Report of a new patient with developmental delay and unusual clinical features 2016 R. SilipigniE. CattaneoM. BaccarinM. Fumagalli + Article (author) -
Impaired Angiogenic Potential of Human Placental Mesenchymal Stromal Cells in Intrauterine Growth Restriction 2016 C. MandòP. RaziniC. NovielliG.M. AnelliS. ErraticoS. BanfiM. MeregalliM. BaccarinY. TorrenteI. Cetin + Article (author) -
Insights into 6q21-q22 : Refinement of the critical region for acro-cardio-facial syndrome 2016 D. MilaniM. BaccarinS. Esposito + Article (author) -
7p22.1 microduplication syndrome : refinement of the critical region 2017 L. RonzoniL. PezzaniA. TucciM. BaccarinS. EspositoD. Milani + Article (author) -
Sequence variants identification at the KCNQ1OT1: TSS differentially Methylated region in isolated omphalocele cases 2017 M. CalvelloL. PaganiniL. PezzaniM. BaccarinL. FontanaS.M. SirchiaL. CanazzaL.L. ColomboF. MoscaS.M. TabanoM.R. Miozzo + Article (author) -
Prenatal upper-limb mesomelia and 2q31.1 microdeletions affecting the regulatory genome 2018 Peron, AngelaBorzani, IreneBaccarin, Marco + Article (author) -
New Insights into Kleefstra Syndrome : Report of Two Novel Cases with Previously Unreported Features and Literature Review 2018 Ciaccio, ClaudiaScuvera, GiuliettaTucci, AriannaGentilin, BarbaraBaccarin, MarcoMarchisio, PaolaMilani, Donatella + Article (author) -
Huntingtin gene CAG repeat size affects autism risk: Family-based and case–control association study 2020 Iennaco R.Baccarin M.Castronovo P.Cucinotta F.Zuccato C.Cattaneo E. + Article (author) -
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