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Natural history of KBG syndrome in a large European cohort:
Loberti, Lorenzo
;
Bruno, Lucia Pia
;
Granata, Stefania
...
Human Molecular Genetics. 31 (2022) 24 - p. 4131-4142 , 2022
Link:
https://doi.org/10.1093/hmg/ddac167
RT Journal T1
Natural history of KBG syndrome in a large European cohort
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddac167&Exemplar=1&LAN=DE A1 Loberti, Lorenzo A1 Bruno, Lucia Pia A1 Granata, Stefania A1 Doddato, Gabriella A1 Resciniti, Sara A1 Fava, Francesca A1 Carullo, Michele A1 Rahikkala, Elisa A1 Jouret, Guillaume A1 Menke, Leonie A A1 Lederer, Damien A1 Vrielynck, Pascal A1 Ryba, Lukáš A1 Brunetti-Pierri, Nicola A1 Lasa-Aranzasti, Amaia A1 Cueto-González, Anna Maria A1 Trujillano, Laura A1 Valenzuela, Irene A1 Tizzano, Eduardo F A1 Spinelli, Alessandro Mauro A1 Bruno, Irene A1 Currò, Aurora A1 Stanzial, Franco A1 Benedicenti, Francesco A1 Lopergolo, Diego A1 Santorelli, Filippo Maria A1 Aristidou, Constantia A1 Tanteles, George A A1 Maystadt, Isabelle A1 Tkemaladze, Tinatin PB Oxford University Press (OUP) YR 2022 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics VO 31 IS 24 SP 4131 OP 4142 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddac167 DO https://doi.org/10.1093/hmg/ddac167 SF ELIB - SuUB Bremen
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