Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation
Crossref DOI link: https://doi.org/10.1136/jmedgenet-2014-102497
Published Online: 2014-07-16
Published Print: 2014-08
Update policy: https://doi.org/10.1136/crossmarkpolicy
Wells, Dagan
Kaur, Kulvinder
Grifo, Jamie
Glassner, Michael
Taylor, Jenny C
Fragouli, Elpida
Munne, Santiago