Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region
Wang, C M, Dixon, P H, Decordova, S, Hodges, M D, Sebire, N J, Ozalp, S, Fallahian, M, Sensi, A, Ashrafi, F, Repiska, V, Zhao, J, Xiang, Y, Savage, P M, Seckl, M J, Fisher, R A
Published in Journal of medical genetics (01.08.2009)
Published in Journal of medical genetics (01.08.2009)
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Journal Article
ASN540SER mutation is associated with a mild form of hypochondroplasia: a 7 years follow-up in an Italian boy
De Sanctis, V, Baldi, M, Marsciani, A, Ravaioli, E, Timoncini, G, Reggiani, L, Sensi, A, Zucchini, A
Published in Georgian medical news (01.09.2012)
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Published in Georgian medical news (01.09.2012)
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An intermediate phenotype between Hay-Wells and Rapp-Hodgkin syndromes in a patient with a novel P63 mutation: confirmation of a variable phenotypic spectrum with a common aetiology
Prontera, P, Escande, F, Cocchi, G, Donti, E, Martini, A, Sensi, A
Published in Genetic counseling (01.01.2008)
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Published in Genetic counseling (01.01.2008)
Journal Article
Mole maker phenotype: possible narrowing of the candidate region
Sensi, A, Gualandi, F, Pittalis, M C, Calabrese, O, Falciano, F, Maestri, I, Bovicelli, L, Calzolari, E
Published in European journal of human genetics : EJHG (01.08.2000)
Published in European journal of human genetics : EJHG (01.08.2000)
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Journal Article
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey
Sensi, A., Cavani, S., Villa, N., Pomponi, M. G., Fogli, A., Gualandi, F., Grasso, M., Sala, E., Pietrobono, R., Baldinotti, F., Savin, E., Ferlini, A., Cecconi, M., Rossi, S., Gallone, S., Bellini, C., Neri, G., Martinoli, E., Simi, P., Dalprà, L., Genuardi, M., Dagna-Bricarelli, F., Calzolari, E.
Published in Prenatal diagnosis (01.08.2004)
Published in Prenatal diagnosis (01.08.2004)
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Journal Article
Paracentric inversion of Yq and review of the literature
Aiello, V, Astolfi, N, Gruppioni, R, Buldrini, B, Prontera, P, Bonfatti, A, Sensi, A, Calzolari, E
Published in Genetic counseling (01.01.2007)
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Published in Genetic counseling (01.01.2007)
Journal Article
Prenatal UPD testing survey in Robertsonian translocations
Gualandi, F., Sensi, A., Trabanelli, C., Falciano, F., Bonfatti, A., Calzolari, E.
Published in Prenatal diagnosis (01.06.2000)
Published in Prenatal diagnosis (01.06.2000)
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Journal Article
Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion
Prontera, P, Aiello, V, Toschi, M, Turci, A, Gruppioni, R, Buldrini, B, Zago, S, Bonfatti, A, Donti, E, Calzolari, E, Sensi, A
Published in Genetic counseling (01.01.2007)
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Published in Genetic counseling (01.01.2007)
Journal Article
Clinical and Radiological Evaluation in Children with Microtia
Calzolari, F., Garani, G., Sensi, A., Martini, A.
Published in British Journal of Audiology (01.10.1999)
Published in British Journal of Audiology (01.10.1999)
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Journal Article
Conference Proceeding
Chromosomal alterations, biological features and in vitro chemosensitivity of SCLC-R1, a new cell line from human metastatic small cell lung carcinoma
Gasperi-Campani, A, Roncuzzi, L, Zoli, W, Lenzi, L, Gruppioni, R, Sensi, A, Zini, N, Farabegoli, F, Amadori, D
Published in European journal of cancer (1990) (01.04.1998)
Published in European journal of cancer (1990) (01.04.1998)
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Journal Article
Prenatal exclusion of UPD from cytogenetic slides: a simple method
Gualandi, F., Sensi, A., Calabrese, O., Gruppioni, R., Pittalis, M. C., Calzolari, E.
Published in Prenatal diagnosis (01.01.1999)
Published in Prenatal diagnosis (01.01.1999)
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Journal Article
Atrial septal defect type Ostium secundum with and without prolonged atrioventricular conduction
Bosi, G, Sensi, A, Scorrano, M, Croci, G, Giusti, S, Calzolari, E
Published in European heart journal (01.12.1995)
Published in European heart journal (01.12.1995)
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A new cell line from human infiltrating ductal carcinoma of the breast: establishment and characterization
Zoli, W, Roncuzzi, L, Flamigni, A, Gruppioni, R, Sensi, A, Zini, N, Amadori, D, Gasperi-Campani, A
Published in Journal of cancer research and clinical oncology (1996)
Published in Journal of cancer research and clinical oncology (1996)
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Journal Article
HLA B51 antigen associated with neutrophil hyper-reactivity
Sensi, A, Gavioli, R, Spisani, S, Balboni, A, Melchiorri, L, Menicucci, A, Palumbo, G, Traniello, S, Baricordi, O R
Published in Disease markers (01.11.1991)
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Published in Disease markers (01.11.1991)
Journal Article
Heteromorphic variant 18ph+ analyzed by sequential CBG and fluorescence in situ hybridization
Sensi, A, Giunta, C, Bonfatti, A, Gruppioni, R, Rubini, M, Fontana, F
Published in Human heredity (01.09.1994)
Published in Human heredity (01.09.1994)
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