المؤلفون: Lauricella, SA, Cuttaia, HS, Vallesi Cardillo, M, Caracausi, CM, Manzella, M, Malacarne, M, PICCIONE, Maria

المساهمون: Lauricella, SA, Cuttaia, HS, Vallesi Cardillo, M, Caracausi, CM, Manzella, M, Malacarne, M, Piccione, M

مصطلحات موضوعية: schizofrenia, riarrangiamenti cromosomici

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3658::3927062da613428312c50431294039e6
http://hdl.handle.net/10447/42906

المؤلفون: Vallesi Cardillo, S, Lauricella, SA, Cuttaia, H, Cavarretta, G, Manzella, CM, Picciotto, F, Cavani, S, Antona, V, CORSELLO, Giovanni, PICCIONE, Maria

المساهمون: Vallesi Cardillo, S, Lauricella, SA, Cuttaia, H, Cavarretta, G, Manzella, CM, Picciotto, F, Cavani, S, Antona, V, Piccione, M, Corsello, G

مصطلحات موضوعية: dup 9p, diagnosi prenatale

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3658::153015bae5a870d7425aea1e63b8837e
http://hdl.handle.net/10447/42070

المؤلفون: Cuttaia, H, Lauricella, SA, Vallesi Cardillo, S, Cavarretta, G, Manzella, CM, Viaggi, C, Consiglio, V, PICCIONE, Maria, CORSELLO, Giovanni

المساهمون: Cuttaia, H, Lauricella, SA, Vallesi Cardillo, S, Cavarretta, G, Manzella, CM, Viaggi, C, Consiglio, V, Piccione, M, Corsello, G

مصطلحات موضوعية: IUGR, Dismorfie cranio-facciali, trisomia 16p

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3658::b321fa4a014010407ad651ad1a4de279
http://hdl.handle.net/10447/42907

المؤلفون: Lauricella, SA, Vallesi Cardillo, S, Cuttaia, H, Cavarretta, G, Manzella, CM, Fiorino, R, Mauro, P, PICCIONE, Maria

المساهمون: Lauricella, SA, Vallesi Cardillo, S, Cuttaia, H, Cavarretta, G, Manzella, CM, Fiorino, R, Mauro, P, Piccione, M

مصطلحات موضوعية: dup 5p, diagnosi prenatale

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3658::7493b713fce16ccea91f8e87c0d1e086
http://hdl.handle.net/10447/42900

المؤلفون: Giardino, D, Corti, C, Ballarati, L, Colombo, D, Sala, E, Villa, N, Piombo, G, Pierluigi, M, Faravelli, F, Guerneri, S, Coviello, D, Lalatta, F, Cavallari, U, Bellotti, D, Barlati, Sergio, Croci, G, Franchi, F, Savin, E, Nocera, G, Amico, Fp, Granata, P, Casalone, R, Nutini, L, Lisi, E, Torricelli, F, Giussani, U, Facchinetti, B, Guanti, G, DI GIACOMO, M, Susca, Fp, Pecile, V, Romitti, L, Cardarelli, L, Racalbuto, E, Police, Ma, Chiodo, F, Rodeschini, O, Falcone, P, Donti, E, Grimoldi, Mg, Martinoli, E, Stioui, S, Caufin, D, Lauricella, Sa, Tanzariello, Sa, Voglino, G, Lenzini, E, Besozzi, M, Larizza, L, Dalprà, L.

المساهمون: Giardino, D, Corti, C, Ballarati, L, Colombo, D, Sala, E, Villa, N, Piombo, G, Pierluigi, M, Faravelli, F, Guerneri, S, Coviello, D, Lalatta, F, Cavallari, U, Bellotti, D, Barlati, S, Croci, G, Franchi, F, Savin, E, Nocera, G, Amico, F, Granata, P, Casalone, R, Nutini, L, Lisi, E, Torricelli, F, Giussani, U, Facchinetti, B, Guanti, G, Di Giacomo, M, Susca, F, Pecile, V, Romitti, L, Cardarelli, L, Racalbuto, E, Police, M, Chiodo, F, Rodeschini, O, Falcone, P, Donti, E, Grimoldi, M, Martinoli, E, Stioui, S, Caufin, D, Lauricella, S, Tanzariello, S, Voglino, G, Lenzini, E, Besozzi, M, Larizza, L, Dalpra', L

المصدر: Prenatal diagnosis. 29(3)

مصطلحات موضوعية: breakpoints distribution, Chromosome Aberrations, Male, prenatal diagnosi, Data Collection, Chromosome Disorders, Amniotic Fluid, Chorionic Villi Sampling, Italy, Pregnancy, Karyotyping, Prenatal Diagnosis, Humans, Female, fragile sites, de novo balanced rearrangement

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::928949598bb92b2c3badcd58f2aab413
https://pubmed.ncbi.nlm.nih.gov/19248039

المؤلفون: Busè M; Department of Sciences for Health Promotion and Mother and Child Care 'Giuseppe D'Alessandro', University of Palermo, Palermo, Italy. mbuse@hotmail.it., Cuttaia HC; Laboratory of Medical Cytogenetic, AOOR Villa Sofia-Cervello, Palermo, Italy., Palazzo D; Regional Referral Centre for Rare Genetic and Chromosomal Diseases, AOOR Villa Sofia-Cervello, Palermo, Italy., Mazara MV; Laboratory of Medical Cytogenetic, AOOR Villa Sofia-Cervello, Palermo, Italy., Lauricella SA; Laboratory of Medical Cytogenetic, AOOR Villa Sofia-Cervello, Palermo, Italy., Malacarne M; S.C. Laboratory of Human Genetics, E.O. Galliera Hospital, Genoa, Italy., Pierluigi M; S.C. Laboratory of Human Genetics, E.O. Galliera Hospital, Genoa, Italy., Cavani S; S.C. Laboratory of Human Genetics, E.O. Galliera Hospital, Genoa, Italy., Piccione M; Department of Sciences for Health Promotion and Mother and Child Care 'Giuseppe D'Alessandro', University of Palermo, Palermo, Italy.

المصدر: Italian journal of pediatrics [Ital J Pediatr] 2017 Jul 19; Vol. 43 (1), pp. 61. Date of Electronic Publication: 2017 Jul 19.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101510759 Publication Model: Electronic Cited Medium: Internet ISSN: 1824-7288 (Electronic) Linking ISSN: 17208424 NLM ISO Abbreviation: Ital J Pediatr Subsets: MEDLINE

مواضيع طبية MeSH: Abnormalities, Multiple/*diagnosis , Megalencephaly/*diagnosis, Child ; Chromosome Deletion ; Chromosomes, Human, Pair 1 ; Female ; Humans ; Infant ; Male ; Phenotype ; Pregnancy ; Prenatal Diagnosis

SCR Disease Name: Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb