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Three cases with de novo 6q imbalance and variable prenatal phenotypeGRATI, Francesca R; LALATTA, Faustina; BALDO, Demetrio et al.American journal of medical genetics. 2005, Vol 136A, Num 3, pp 254-258, issn 0148-7299, 5 p.Article

Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosisLALATTA, Faustina; QUAGLIARINI, Donatella; NARETTO, Valeria Giorgia et al.European journal of pediatrics. 2010, Vol 169, Num 10, pp 1255-1261, issn 0340-6199, 7 p.Article

Expanding the phenotype of 22q13.3 deletion : report of a case detected prenatallyMAITZ, Silvia; GENTILIN, Barbara; COLLI, Anna Maria et al.Prenatal diagnosis. 2008, Vol 28, Num 10, pp 978-980, issn 0197-3851, 3 p.Article

Preferential X Chromosome Loss But Random Inactivation Characterize Primary Biliary CirrhosisMIOZZO, Monica; SELMI, Carlo; GENTILIN, Barbara et al.Hepatology (Baltimore, Md.). 2007, Vol 46, Num 2, pp 456-462, issn 0270-9139, 7 p.Article

Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnanciesGRATI, Francesca R; SIRCHIA, Silvia M; MIOZZO, Monica et al.European journal of human genetics. 2004, Vol 12, Num 4, pp 272-278, issn 1018-4813, 7 p.Article