A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangements
1q42.12-qter区域同时存在重复、三重复和单亲二体性的病例支持微同源介导的断裂诱导复制模型,用于解释复制重排。
期刊:Molecular Cytogenetics
影响因子:1.4
doi:10.1186/s13039-017-0316-6
Kohmoto, Tomohiro; Okamoto, Nana; Naruto, Takuya; Murata, Chie; Ouchi, Yuya; Fujita, Naoko; Inagaki, Hidehito; Satomura, Shigeko; Okamoto, Nobuhiko; Saito, Masako; Masuda, Kiyoshi; Kurahashi, Hiroki; Imoto, Issei