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- W2021504967 abstract "Our hypothesis is that a massively parallel shot gun sequencing based method could provide higher resolution chromosome copy number variation (CNV) testing at a cost more acceptable for preimplantation genetic diagnosis." @default.
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- W2021504967 date "2014-09-01" @default.
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- W2021504967 title "Copy number variation sequencing for diagnosis of chromosome abnormalities in pre-implantation embryos" @default.
- W2021504967 doi "https://doi.org/10.1016/j.fertnstert.2014.07.619" @default.
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