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Item Statistics
Familial STAG2 germline mutation defines a new human cohesinopathy
Repository | University of Melbourne [Minerva Access] |
URL | http://hdl.handle.net/11343/216412 |
Author(s) | orcid:0000-0001-7879-0450; orcid:0000-0001-8770-8009; orcid:0000-0003-2948-2413; Soardi, FC; Machado-Silva, A; Linhares, ND; Zheng, G; Qu, Q; Pena, HB; Martins, TMM; Vieira, HGS; Pereira, NB; Melo-Minardi, RC; Gomes, CC; Gomez, RS; Gomes, DA; Pires, DEV; |
Item type | Article |
Journal | Npj Genomic Medicine, Online_ISSN:2056-7944 |
DOI | https://doi.org/10.1038/s41525-017-0009-4 |