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Genome sequencing of human in vitro fertilisation embryos for pathogenic variation screening
Whole-genome sequencing of preimplantation human embryos to detect and screen for genetic diseases is a technically challenging extension to preconception screening. Combining preconception genetic screening with preimplantation testing of human embryos facilitates the detection of de novo mutations...
Autores principales: | Murphy, Nicholas M., Samarasekera, Tanya S., Macaskill, Lisa, Mullen, Jayne, Rombauts, Luk J. F. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052235/ https://www.ncbi.nlm.nih.gov/pubmed/32123222 http://dx.doi.org/10.1038/s41598-020-60704-0 |
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