GENTILIN, BARBARA

GENTILIN, BARBARA  

Universita' degli Studi di MILANO  

Risultati 1 - 11 di 11 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva 1-gen-2005 B. GentilinF.R. GratiP. InvernizziC. SelmiS.M. SirchiaF. RossellaG. SimoniM. Miozzo + Book Part (author) -
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies 1-gen-2004 F.R. GratiS.M. SirchiaB. GentilinF. RossellaL. RamoscelliG. BulfamanteI. CetinG. SimoniM. Miozzo + Article (author) -
Congenital diaphragmatic hernia as prenatal presentation of Apert syndrome 1-set-2011 G.P. BulfamanteL. AvaglianoI. FabiettiB. Gentilin + Article (author) -
Dysmorphologic assessment in 115 Mayer-Rokitansky-Küster-Hauser patients 1-lug-2015 F. MottaE. RestelliM. MiozzoC. GervasiniB. GentilinL. Fedele + Article (author) -
Echocardiographic indications to detect chromosome 22 microdeletions through invasive prenatal procedures 1-gen-2007 M. INFANTINOB. GENTILINL. MANDIAI. CETIN + Article (author) -
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies 1-gen-2005 F.R. GratiM. MiozzoF. RossellaP. AntonazzoB. GentilinS.M. SirchiaS. RiganoG. BulfamanteI. CetinG. Simoni + Article (author) -
New Insights into Kleefstra Syndrome : Report of Two Novel Cases with Previously Unreported Features and Literature Review 17-nov-2018 Ciaccio, ClaudiaScuvera, GiuliettaTucci, AriannaGentilin, BarbaraBaccarin, MarcoMarchisio, PaolaMilani, Donatella + Article (author) -
Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis 1-ago-2007 M.R. MiozzoC.F. SelmiB. GentilinF.R. GratiS.M. SirchiaM. ZuinM. PoddaP. Invernizzi + Article (author) -
Prenatal/neonatal pathology findings in two cases of Cornelia de Lange syndrome harboring novel mutations of NIPBL 1-mar-2007 B. GentilinM. MasciadriC. GervasiniBENTIVEGNA, ANGELAP. CastronovoL. Larizza + Article (author) -
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome 5-ago-2013 M. CalvelloS. TabanoP. ColapietroS. MaitzPANSA, ALESSANDRAC. AugelloB. GentilinL. LarizzaS.M. SirchiaM. Miozzo + Article (author) -
Three cases with de novo 6q imbalance and variable prenatal phenotype 30-lug-2005 FR GratiB GentilinF RossellaI CetinG SimoniM Miozzo + Article (author) -