المؤلفون: Costanza J., Camanni M., Ferrari M. M., De Cosmi V., Tabano S., Fontana L., Radaelli T., Privitera G., Alberico D., Colapietro P., Motta S., Sirchia S., Stampalija T., Tabasso C., Roggero P., Parazzini F., Mosca F., Ferrazzi E., Bosari S., Miozzo M., Agostoni C.

المساهمون: Costanza, J., Camanni, M., Ferrari, M. M., De Cosmi, V., Tabano, S., Fontana, L., Radaelli, T., Privitera, G., Alberico, D., Colapietro, P., Motta, S., Sirchia, S., Stampalija, T., Tabasso, C., Roggero, P., Parazzini, F., Mosca, F., Ferrazzi, E., Bosari, S., Miozzo, M., Agostoni, C.

مصطلحات موضوعية: n/a

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34344991; info:eu-repo/semantics/altIdentifier/wos/WOS:000680759200001; volume:91; issue:7; firstpage:1890; lastpage:1896; numberofpages:7; journal:PEDIATRIC RESEARCH; http://hdl.handle.net/11368/2993922Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85111928550; https://www.nature.com/articles/s41390-021-01665-6Test

الإتاحة: https://doi.org/10.1038/s41390-021-01665-6Test
http://hdl.handle.net/11368/2993922Test
https://www.nature.com/articles/s41390-021-01665-6Test

المؤلفون: Cerrato F., Sparago A., Ariani F., Brugnoletti F., Calzari L., Coppede F., De Luca A., Gervasini C., Giardina E., Gurrieri F., Nigro C. L., Merla G., Miozzo M., Russo S., Sangiorgi E., Sirchia S. M., Squeo G. M., Tabano S., Tabolacci E., Torrente I., Genuardi M., Neri G., Riccio A.

المساهمون: Cerrato, F., Sparago, A., Ariani, F., Brugnoletti, F., Calzari, L., Coppede, F., De Luca, A., Gervasini, C., Giardina, E., Gurrieri, F., Nigro, C. L., Merla, G., Miozzo, M., Russo, S., Sangiorgi, E., Sirchia, S. M., Squeo, G. M., Tabano, S., Tabolacci, E., Torrente, I., Genuardi, M., Neri, G., Riccio, A.

مصطلحات موضوعية: Developmental delay/intellectual disability disorder, DNA methylation, Epi-signature, Genetic testing, Hereditary tumor, High-throughput analysi, Imprinting disorder, Neuromuscular disease, Prenatal diagnosis

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32224912; info:eu-repo/semantics/altIdentifier/wos/WOS:000537224600081; volume:11; issue:4; firstpage:355; numberofpages:30; journal:GENES; https://hdl.handle.net/11568/1041052Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85082574850; https://www.mdpi.com/2073-4425/11/4/355Test

الإتاحة: https://doi.org/10.3390/genes11040355Test
https://hdl.handle.net/11568/1041052Test
https://www.mdpi.com/2073-4425/11/4/355Test

المؤلفون: Fontana L., Tabano S., Maitz S., Colapietro P., Garzia E., Gerli A. G., Sirchia S. M., Miozzo M.

المساهمون: L. Fontana, S. Tabano, S. Maitz, P. Colapietro, E. Garzia, A.G. Gerli, S.M. Sirchia, M. Miozzo

مصطلحات موضوعية: Beckwith-Wiedemann syndrome, Clinical diagnosi, Discordant monozygotic twin, Molecular testing, Multilocus imprinting disturbance, X-chromosome inactivation, Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33810554; info:eu-repo/semantics/altIdentifier/wos/WOS:000638646600001; volume:22; issue:7; firstpage:1; lastpage:20; numberofpages:20; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; http://hdl.handle.net/2434/851677Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85103053768

الإتاحة: https://doi.org/10.3390/ijms22073445Test
http://hdl.handle.net/2434/851677Test

المؤلفون: Rondinone O., Murgia A., Costanza J., Tabano S., Camanni M., Corsaro L., Fontana L., Colapietro P., Calzari L., Motta S., Santaniello C., Radaelli T., Ferrazzi E., Bosari S., Gentilini D., Sirchia S. M., Miozzo M.

المساهمون: O. Rondinone, A. Murgia, J. Costanza, S. Tabano, M. Camanni, L. Corsaro, L. Fontana, P. Colapietro, L. Calzari, S. Motta, C. Santaniello, T. Radaelli, E. Ferrazzi, S. Bosari, D. Gentilini, S.M. Sirchia, M. Miozzo

مصطلحات موضوعية: birth weight, LINE-1, methylome, normal pregnancie, placenta, Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33669975; info:eu-repo/semantics/altIdentifier/wos/WOS:000623926500001; volume:22; issue:4; firstpage:1; lastpage:19; numberofpages:19; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; http://hdl.handle.net/2434/826856Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85100921870

الإتاحة: https://doi.org/10.3390/ijms22042136Test
http://hdl.handle.net/2434/826856Test

المؤلفون: Rovina D., La Vecchia M., Cortesi A., Fontana L., Pesant M., Maitz S., Tabano S., Bodega B., Miozzo M., Sirchia S. M.

المساهمون: D. Rovina, M. La Vecchia, A. Cortesi, L. Fontana, M. Pesant, S. Maitz, S. Tabano, B. Bodega, M. Miozzo, S.M. Sirchia

مصطلحات موضوعية: Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32427849; info:eu-repo/semantics/altIdentifier/wos/WOS:000540568100068; volume:10; issue:1; journal:SCIENTIFIC REPORTS; http://hdl.handle.net/2434/738695Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85084964861

الإتاحة: https://doi.org/10.1038/s41598-020-65082-1Test
http://hdl.handle.net/2434/738695Test

المؤلفون: Fontana L., Bedeschi M. F., Cagnoli G. A., Costanza J, Persico N., Gangi S., Porro M., Ajmone P., Colapietro P., Santaniello C., Crippa M., Sirchia s. m., Miozzo M., Tabano S.

المساهمون: L. Fontana, M.F. Bedeschi, G.A. Cagnoli, J. Costanza, N. Persico, S. Gangi, M. Porro, P. Ajmone, P. Colapietro, C. Santaniello, M. Crippa, S.M. Sirchia, M. Miozzo, S. Tabano

مصطلحات موضوعية: Beckwith-Wiedemann Syndrome, X-chromosome inactivation, prenatal diagnosi, twin, whole exome sequencing, Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32627967; info:eu-repo/semantics/altIdentifier/wos/WOS:000545402700001; volume:8; issue:9; firstpage:1; lastpage:12; numberofpages:12; journal:MOLECULAR GENETICS & GENOMIC MEDICINE; http://hdl.handle.net/2434/772021Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85087568804

الإتاحة: https://doi.org/10.1002/mgg3.1386Test
http://hdl.handle.net/2434/772021Test

المؤلفون: 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.

المساهمون: Ministero della Salute and Regione Lombardia, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Flagship ‘InterOmics’, Fondazione Regionale per la Ricerca Biomedica

المصدر: Epigenetics ; volume 13, issue 9, page 897-909 ; ISSN 1559-2294 1559-2308

الإتاحة: https://doi.org/10.1080/15592294.2018.1514230Test

المؤلفون: Pileggi S., La Vecchia M., Colombo E. A., Fontana L., Colapietro P., Rovina D., Morotti A., Tabano S., Porta G., Alcalay M., Gervasini C., Miozzo M., Sirchia S. M.

المساهمون: Pileggi, S., La Vecchia, M., Colombo, E. A., Fontana, L., Colapietro, P., Rovina, D., Morotti, A., Tabano, S., Porta, G., Alcalay, M., Gervasini, C., Miozzo, M., Sirchia, S. M.

مصطلحات موضوعية: 3D chromatin conformation, Cohesin, Cornelia de Lange Syndrome, IGF2/H19 domain, Imprinted gene, WNT pathway

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000727593200001; volume:11; issue:11; firstpage:1622; journal:BIOMOLECULES; https://hdl.handle.net/11383/2131581Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85118250754

الإتاحة: https://doi.org/10.3390/biom11111622Test
https://hdl.handle.net/11383/2131581Test

المؤلفون: Pagani I.S., Terrinoni A., Marenghi L., Zucchi I., Chiaravalli A.M., Serra V., ROVERA, FRANCESCA ANGELA, Sirchia S., DIONIGI, GIANLORENZO, Miozzo M., Frattini A., Ferrari A., CAPELLA, CARLO RENATO, PASQUALI, FRANCESCO, LO CURTO, FRANCESCO, Albertini A., Melino G., PORTA, GIOVANNI

المساهمون: Pagani, I. S., Terrinoni, A., Marenghi, L., Zucchi, I., Chiaravalli, A. M., Serra, V., Rovera, FRANCESCA ANGELA, Sirchia, S., Dionigi, Gianlorenzo, Miozzo, M., Frattini, A., Ferrari, A., Capella, CARLO RENATO, Pasquali, Francesco, LO CURTO, Francesco, Albertini, A., Melino, G., Porta, Giovanni

مصطلحات موضوعية: otx 1 breast cancer

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000283986900016; volume:16; issue:suppl 1; firstpage:53; lastpage:56; journal:THE BREAST JOURNAL; http://hdl.handle.net/11383/1916725Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-78649293646

الإتاحة: http://hdl.handle.net/11383/1916725Test

المؤلفون: Terrinoni, A, Pagani, I S, Zucchi, I, Chiaravalli, A M, Serra, V, Rovera, F, Sirchia, S, Dionigi, G, Miozzo, M, Frattini, A, Ferrari, A, Capella, C, Pasquali, F, Lo Curto, F, Albertini, A, Melino, G, Porta, G

مصطلحات موضوعية: Cancer Research, Genetics, Molecular Biology

العلاقة: url:https://www.openaccessrepository.it/communities/itmirrorTest; https://www.openaccessrepository.it/record/156114Test

الإتاحة: https://doi.org/10.1038/onc.2013.572Test
https://www.openaccessrepository.it/record/156114Test