Additional file 3: Table S3. of A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangements

Autor: Kohmoto, Tomohiro, Okamoto, Nana, Naruto, Takuya, Murata, Chie, Ouchi, Yuya, Fujita, Naoko, Hidehito Inagaki, Satomura, Shigeko, Okamoto, Nobuhiko, Saito, Masako, Masuda, Kiyoshi, Kurahashi, Hiroki, Imoto, Issei
Rok vydání: 2017
Předmět:
DOI: 10.6084/m9.figshare.c.3767561_d3.v1
Popis: Autosomal recessive diseases and causative genes aound the isoUPD region. (DOCX 14 kb)
Databáze: OpenAIRE