GENTILIN, BARBARA
GENTILIN, BARBARA
Universita' degli Studi di MILANO
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva
2005-01-01 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
2004-01-01 F.R. Grati, S.M. Sirchia, B. Gentilin, F. Rossella, L. Ramoscelli, P. Antonazzo, U. Cavallari , G. Bulfamante, I. Cetin , G. Simoni, M. Miozzo
Dysmorphologic assessment in 115 Mayer-Rokitansky-Küster-Hauser patients
2015-07-01 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
2007-01-01 M. Infantino, B. Gentilin, E. Brandolisio, A. Colli, L. Mauri, L. Mandia, A. Kustermann, I. Cetin
New Insights into Kleefstra Syndrome : Report of Two Novel Cases with Previously Unreported Features and Literature Review
2018-11-17 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
2007-08-01 M.R. Miozzo, C.F. Selmi, B. Gentilin, F.R. Grati, S.M. Sirchia, M. Zuin, M.E. Gershwin, M. Podda, P. Invernizzi
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
2013-08-05 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