Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders
Fontana, L., Bedeschi, M. F., Maitz, S., Cereda, A., Faré, C., Motta, S., Seresini, A., D'Ursi, P., Orro, A., Pecile, V., Calvello, M., Selicorni, A., Lalatta, F., Milani, D., Sirchia, S. M., Miozzo, M., Tabano, S.
Published in Epigenetics (02.09.2018)
Published in Epigenetics (02.09.2018)
Get full text
Journal Article
Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients
De Gregori, M, Ciccone, R, Magini, P, Pramparo, T, Gimelli, S, Messa, J, Novara, F, Vetro, A, Rossi, E, Maraschio, P, Bonaglia, M C, Anichini, C, Ferrero, G B, Silengo, M, Fazzi, E, Zatterale, A, Fischetto, R, Previderé, C, Belli, S, Turci, A, Calabrese, G, Bernardi, F, Meneghelli, E, Riegel, M, Rocchi, M, Guerneri, S, Lalatta, F, Zelante, L, Romano, C, Fichera, M, Mattina, T, Arrigo, G, Zollino, M, Giglio, S, Lonardo, F, Bonfante, A, Ferlini, A, Cifuentes, F, Van Esch, H, Backx, L, Schinzel, A, Vermeesch, J R, Zuffardi, O
Published in Journal of medical genetics (01.12.2007)
Published in Journal of medical genetics (01.12.2007)
Get full text
Journal Article
Bone involvement and mineral metabolism in Williams’ syndrome
Palmieri, S., Bedeschi, M. F., Cairoli, E., Morelli, V., Lunati, M. E., Scillitani, A., Carnevale, V., Lalatta, F., Barbieri, A. M., Orsi, E., Spada, A., Chiodini, I., Eller-Vainicher, C.
Published in Journal of endocrinological investigation (01.03.2019)
Published in Journal of endocrinological investigation (01.03.2019)
Get full text
Journal Article
P22.02: Postmortem high resolution (HR) magnetic resonance imaging (MRI) in fetuses with brain abnormalities and confirmation of in utero MRI findings
Scola, E., Lombardi, S., Avignone, S., Cinnante, C., Boito, S.M., Lalatta, F., Fogliani, R., Persico, N., Triulzi, F.
Published in Ultrasound in obstetrics & gynecology (01.09.2016)
Published in Ultrasound in obstetrics & gynecology (01.09.2016)
Get full text
Journal Article
Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 gene
Gentilin, B., Forzano, F., Bedeschi, M. F., Rizzuti, T., Faravelli, F., Izzi, C., Lituania, M., Rodriguez‐Perez, C., Bondioni, M. P., Savoldi, G., Grosso, E., Botta, G., Viora, E., Baffico, A. M., Lalatta, F.
Published in Ultrasound in obstetrics & gynecology (01.09.2010)
Published in Ultrasound in obstetrics & gynecology (01.09.2010)
Get full text
Journal Article
Double Pituitary and Conserved Function in an Adult Patient with Neurofibromatosis Type 1
Filopanti, M, Verga, U, Ermetici, F, Natacci, F, Lalatta, F, Avignone, S, Trespidi, L, Beck-Peccoz, P, Mantovani, G, Lania, A. G, Spada, A
Published in The journal of clinical endocrinology and metabolism (01.07.2011)
Published in The journal of clinical endocrinology and metabolism (01.07.2011)
Get full text
Journal Article
P33.07: Congenital genu recurvatum with dislocation of the knees: a case report
Boito, S., Mandia, L., Lalatta, F., Ossola, W., Colombo, L., Mosca, F., Pardi, G.
Published in Ultrasound in obstetrics & gynecology (01.10.2007)
Published in Ultrasound in obstetrics & gynecology (01.10.2007)
Get full text
Journal Article
The role of integrated imaging techniques for prenatal prediction of phenotype in two cases of facial anomalies
Rustico, M. A., Lalatta, F., Righini, A., Spaccini, L., Fabietti, I., Nicolini, U.
Published in Prenatal diagnosis (01.07.2004)
Published in Prenatal diagnosis (01.07.2004)
Get full text
Journal Article
Cumming syndrome with heterotaxia, campomelia and absent uterus/fallopian tubes
Bedeschi, M.F., Spaccini, L., Rizzuti, T., Coviello, D.A., Castorina, P., Natacci, F., Lalatta, F.
Published in American journal of medical genetics. Part A (30.01.2005)
Published in American journal of medical genetics. Part A (30.01.2005)
Get full text
Journal Article
60. FOUR YEARS EXPERIENCE OF PREIMPLANTATION GENETIC TESTING OF FOUR MONOGENIC DISORDERS (CYSTIC FIBROSIS, BETA-THALASSAEMIA, HEMOPHILIA A AND B)
Mortarino, M., Biffignandi, A., Seia, M., Restelli, L., Riccaboni, A., Bianchi, V., Lalatta, F., Somigliana, E., Peyvandi, F.
Published in Reproductive biomedicine online (01.08.2019)
Published in Reproductive biomedicine online (01.08.2019)
Get full text
Journal Article
Nasopharyngeal teratoma and diaphragmatic hernia: a non random association?
Natacci, F, Moschetta, M, Bedeschi, M F, Spaccini, L, Capelli, A, Segni, M Di, Rizzuti, T, Mosca, F, Lalatta, F
Published in Clinical dysmorphology (01.10.2004)
Published in Clinical dysmorphology (01.10.2004)
Get more information
Journal Article
Prenatal diagnosis of JAK3 deficient SCID
Schumacher, R. F., Mella, P., Lalatta, F., Fiorini, M., Giliani, S., Villa, A., Candotti, F., Notarangelo, Luigi D.
Published in Prenatal diagnosis (01.07.1999)
Published in Prenatal diagnosis (01.07.1999)
Get full text
Journal Article
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis
Giliani, S., Fiorini, M., Mella, P., Candotti, F., Schumacher, R. F., Wengler, G. S., Lalatta, F., Fasth, A., Badolato, R., Ugazio, A. G., Albertini, A., Notarangelo, L. D.
Published in Prenatal diagnosis (01.01.1999)
Published in Prenatal diagnosis (01.01.1999)
Get full text
Journal Article
Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism
Sirchia, S. M., Garagiola, I., Colucci, G., Guerneri, S., Lalatta, F., Grimoldi, M. G., Simoni, G.
Published in Prenatal diagnosis (01.03.1998)
Published in Prenatal diagnosis (01.03.1998)
Get full text
Journal Article
SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome
Gervasini, Cristina, Grati, Francesca Romana, Lalatta, Faustina, Tabano, Silvia, Gentilin, Barbara, Colapietro, Patrizia, De Toffol, Simona, Frontino, Giada, Motta, Francesca, Maitz, Silvia, Bernardini, Laura, Dallapiccola, Bruno, Fedele, Luigi, Larizza, Lidia, Miozzo, Monica
Published in Genetics in medicine (01.10.2010)
Published in Genetics in medicine (01.10.2010)
Get full text
Journal Article
First-trimester prenatal diagnosis of Roberts syndrome
Stioui, S, Privitera, O, Brambati, B, Zuliani, G, Lalatta, F, Simoni, G
Published in Prenatal diagnosis (01.02.1992)
Published in Prenatal diagnosis (01.02.1992)
Get more information
Journal Article
Trisomy 10qter confirmed by in situ hybridisation
Briscioli, V, Floridia, G, Rossi, E, Selicorni, A, Lalatta, F, Zuffardi, O
Published in Journal of medical genetics (01.07.1993)
Published in Journal of medical genetics (01.07.1993)
Get full text
Journal Article