Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case report
Crossref DOI link: https://0-doi-org.brum.beds.ac.uk/10.1186/s12881-014-0125-2
Published Online: 2014-11-25
Published Print: 2014-12
Update policy: https://0-doi-org.brum.beds.ac.uk/10.1007/springer_crossmark_policy
Luo, Shiyu
Huang, Wen
Xia, Qiuping
Xia, Yan
Du, Qian
Wu, Lingqian
Duan, Ranhui
License valid from 2014-11-25
Article History
Received: 3 July 2014
Accepted: 4 November 2014
First Online: 25 November 2014