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:	genetic structures sense organs musculoskeletal system human activities eye diseases
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
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::408f93efede6db066254cae85f98cf7f Zobrazit plný text záznamu