GENTILIN, BARBARA
GENTILIN, BARBARA
Universita' degli Studi di MILANO
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva
2005 B. Gentilin, F.R. Grati, P. Invernizzi, C. Selmi, P. Busatto, S.M. Sirchia, F. Rossella, G. Simoni, M. Miozzo
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies
2004 F.R. Grati, S.M. Sirchia, B. Gentilin, F. Rossella, L. Ramoscelli, P. Antonazzo, U. Cavallari , G. Bulfamante, I. Cetin , G. Simoni, M. Miozzo
Congenital diaphragmatic hernia as prenatal presentation of Apert syndrome
2011 G.P. Bulfamante, S. Gana, L. Avagliano, I. Fabietti, B. Gentilin, F. Lalatta
Dysmorphologic assessment in 115 Mayer-Rokitansky-Küster-Hauser patients
2015 F. Lalatta, F. Motta, E. Restelli, M. Bellini, M. Miozzo, C. Gervasini, B. Dallapiccola, B. Gentilin, L. Fedele
Echocardiographic indications to detect chromosome 22 microdeletions through invasive prenatal procedures
2007 M. Infantino, B. Gentilin, E. Brandolisio, A. Colli, L. Mauri, L. Mandia, A. Kustermann, I. Cetin
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies
2005 F.R. Grati, M. Miozzo, B. Cassani, F. Rossella, P. Antonazzo, B. Gentilin, S.M. Sirchia, L. Mori, S. Rigano, G. Bulfamante, I. Cetin, G. Simoni
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
Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis
2007 M.R. Miozzo, C.F. Selmi, B. Gentilin, F.R. Grati, S.M. Sirchia, M. Zuin, M.E. Gershwin, M. Podda, P. Invernizzi
Prenatal/neonatal pathology findings in two cases of Cornelia de Lange syndrome harboring novel mutations of NIPBL
2007 F. Lalatta, S. Russo, B. Gentilin, L. Spaccini, C. Boschetto, F. Cavalleri, M. Masciadri, C. Gervasini, A. Bentivegna, P. Castronovo, L. Larizza
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
2013 M. Calvello, S. Tabano, P. Colapietro, S. Maitz, A. Pansa, C. Augello, F. Lalatta, B. Gentilin, F. Spreafico, L. Calzari, D. Perotti, L. Larizza, S. Russo, A. Selicorni, S.M. Sirchia, M. Miozzo
Three cases with de novo 6q imbalance and variable prenatal phenotype
2005 FR Grati ,F Lalatta ,L Turolla ,U Cavallari ,B Gentilin ,F Rossella ,I Cetin ,P Antonazzo ,M Bellotti ,F Dulcetti ,D Baldo,R Tenconi,G Simoni,M Miozzo