Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation

BACKGROUND: The majority of human embryos created using in vitro fertilisation (IVF) techniques are aneuploid. Comprehensive chromosome screening methods, applicable to single cells biopsied from preimplantation embryos, allow reliable identification and transfer of euploid embryos. Recently, random...

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Detalles Bibliográficos
Autores principales: Wells, Dagan, Kaur, Kulvinder, Grifo, Jamie, Glassner, Michael, Taylor, Jenny C, Fragouli, Elpida, Munne, Santiago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Methods
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112454/
https://www.ncbi.nlm.nih.gov/pubmed/25031024
http://dx.doi.org/10.1136/jmedgenet-2014-102497

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112454/
https://www.ncbi.nlm.nih.gov/pubmed/25031024
http://dx.doi.org/10.1136/jmedgenet-2014-102497

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