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HeterozygousHMGB1loss‐of‐function variants are associated w..:
Uguen, Kévin
;
Krysiak, Kilannin
;
Audebert‐Bellanger, Séverine
...
Clinical Genetics. 100 (2021) 4 - p. 386-395 , 2021
Link:
https://doi.org/10.1111/cge.14015
RT Journal T1
HeterozygousHMGB1loss‐of‐function variants are associated with developmental delay and microcephaly
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.14015&Exemplar=1&LAN=DE A1 Uguen, Kévin A1 Krysiak, Kilannin A1 Audebert‐Bellanger, Séverine A1 Redon, Sylvia A1 Benech, Caroline A1 Viora‐Dupont, Eléonore A1 Tran Mau‐Them, Frederic A1 Rondeau, Sophie A1 Elsharkawi, Ibrahim A1 Granadillo, Jorge L. A1 Neidich, Julie A1 Soares, Celia Azevedo A1 Tkachenko, Natáliya A1 M. Amudhavalli, Shivarajan A1 Engleman, Kendra A1 Boland, Anne A1 Deleuze, Jean‐François A1 Bezieau, Stéphane A1 Odent, Sylvie A1 Toutain, Annick A1 Bonneau, Dominique A1 Gilbert‐Dussardier, Brigitte A1 Faivre, Laurence A1 Rio, Marlène A1 Le Marechal, Cedric A1 Ferec, Claude A1 Repnikova, Elena A1 Cao, Yang PB Wiley YR 2021 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 100 IS 4 SP 386 OP 395 LK http://dx.doi.org/https://doi.org/10.1111/cge.14015 DO https://doi.org/10.1111/cge.14015 SF ELIB - SuUB Bremen
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