المؤلفون: Trajkova, Slavica, Kerkhof, Jennifer, Sebastiano, Matteo Rossi, Pavinato, Lisa, Ferrero, Enza, Giovenino, Chiara, Carli, Diana, Di Gregorio, Eleonora, Marinoni, Roberta, Mandrile, Giorgia, Palermo, Flavia, Carestiato, Silvia, Cardaropoli, Simona, Pullano, Verdiana, Rinninella, Antonina, Giorgio, Elisa, Pippucci, Tommaso, Dimartino, Paola, Rzasa, Jessica, Rooney, Kathleen, McConkey, Haley, Petlichkovski, Aleksandar, Pasini, Barbara, Sukarova-Angelovska, Elena, Campbell, Christopher M, Metcalfe, Kay, Jenkinson, Sarah, Banka, Siddharth, Mussa, Alessandro, Ferrero, Giovanni Battista, Sadikovic, Bekim, Brusco, Alfredo

المصدر: Trajkova , S , Kerkhof , J , Sebastiano , M R , Pavinato , L , Ferrero , E , Giovenino , C , Carli , D , Di Gregorio , E , Marinoni , R , Mandrile , G , Palermo , F , Carestiato , S , Cardaropoli , S , Pullano , V , Rinninella , A , Giorgio , E , Pippucci , T , Dimartino , P , Rzasa , J , Rooney , K , McConkey , H , Petlichkovski , A , Pasini , B , Sukarova-Angelovska , E , Campbell ....

مصطلحات موضوعية: ARID1A, ARID1B, BAFopathy, Coffin-Siris syndrome, DNA methylation, SMARCA2, SMARCA4, SMARCB1, episignatures, neurodevelopmental disorders

Relation: https://research.manchester.ac.uk/en/publications/84163720-c2ef-4382-b846-8147e8ac1305

الاتاحة: https://research.manchester.ac.uk/en/publications/84163720-c2ef-4382-b846-8147e8ac1305
https://doi.org/10.1016/j.xhgg.2024.100309
http://www.scopus.com/inward/record.url?scp=85195079453&partnerID=8YFLogxK
https://www.mendeley.com/catalogue/ec41d092-5e5b-39a3-a6de-cd3033d2a779/

المؤلفون: Giovenino, Chiara, Trajkova, Slavica, Pavinato, Lisa, Cardaropoli, Simona, Pullano, Verdiana, Ferrero, Enza, Sukarova-Angelovska, Elena, Carestiato, Silvia, Salmin, Paola, Rinninella, Antonina, Battaglia, Anthony, Bertoli, Luca, Fadda, Antonio, Palermo, Flavia, Carli, Diana, Mussa, Alessandro, Dimartino, Paola, Bruselles, Alessandro, Froukh, Tawfiq, Mandrile, Giorgia, Pasini, Barbara, De Rubeis, Silvia, Buxbaum, Joseph D, Pippucci, Tommaso, Tartaglia, Marco, Rossato, Marzia, Delledonne, Massimo, Ferrero, Giovanni Battista, Brusco, Alfredo

المساهمون: Giovenino, Chiara, Trajkova, Slavica, Pavinato, Lisa, Cardaropoli, Simona, Pullano, Verdiana, Ferrero, Enza, Sukarova-Angelovska, Elena, Carestiato, Silvia, Salmin, Paola, Rinninella, Antonina, Battaglia, Anthony, Bertoli, Luca, Fadda, Antonio, Palermo, Flavia, Carli, Diana, Mussa, Alessandro, Dimartino, Paola, Bruselles, Alessandro, Froukh, Tawfiq, Mandrile, Giorgia, Pasini, Barbara, De Rubeis, Silvia, Buxbaum, Joseph D, Pippucci, Tommaso, Tartaglia, Marco, Rossato, Marzia, Delledonne, Massimo, Ferrero, Giovanni Battista, Brusco, Alfredo

مصطلحات موضوعية: neurodevelopmental disorde, X skewed inactivation, X linked disorders, exome, Xdrop long-DNA technology

Relation: info:eu-repo/semantics/altIdentifier/pmid/36879111; info:eu-repo/semantics/altIdentifier/wos/WOS:000944081800001; firstpage:1; lastpage:9; numberofpages:9; journal:EUROPEAN JOURNAL OF HUMAN GENETICS; https://hdl.handle.net/2318/1903052; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85149409681; https://www.nature.com/articles/s41431-023-01324-w

الاتاحة: https://hdl.handle.net/2318/1903052
https://doi.org/10.1038/s41431-023-01324-w
https://www.nature.com/articles/s41431-023-01324-w